Data Sheet
Sterilizing-grade Durapore®
0.1 μm and 0.22 μm Hydrophilic Filters
Superior filters for the sterile filtration
of biopharmaceutical liquids
A trusted name in the industry for
over 30 years, Durapore® sterilizinggrade 0.1 μm and 0.22 μm hydrophilic
polyvinylidene fluoride (PVDF)
membranes are low protein binding
and provide sterility assurance, high
flow rates and throughputs.
The Durapore® membrane contributes
to clean processes due to low extractables, broad chemical compatibility,
and its non-fiber releasing properties.
Membrane Types
Durapore® hydrophilic membrane
• 0.1 μm hydrophilic
Benefits
• 0.22 μm hydrophilic
•
Low protein binding membrane yields high protein
recovery with minimal loss of valuable product
Filter Formats
•
Superior membrane for filtration processes
requiring high flow rates and throughputs
•
Millipak® low-volume capsule filters
•
Ideal for designing scalable solutions from bench
top to full-scale manufacturing
•
OptiScale® small-scale disposable capsule filters
•
Opticap® XL and XLT disposable capsule filters
•
Cartridge filters
EMD Millipore Corp. is a subsidiary of Merck KGaA, Darmstadt, Germany
Regulatory Compliance
Multiple Formats Available
Filters with hydrophilic Durapore® membranes are
designed, developed, and manufactured in accordance
with a Quality Management System approved by an
accredited registering body to an ISO® 9001 Quality
Systems Standard. Each Durapore® filter is shipped
with a Certificate of Quality. Each cartridge filter and
Millipak®, Opticap® XL and Opticap® XLT capsule filter
is integrity tested during manufacturing and is supported with a Validation Guide for compliance with
regulatory requirements. For traceability and easy
identification, each device is marked with the product
name and identifying characteristics.
Sterilizing-grade hydrophilic Durapore® membranes are
available in four formats, two pore sizes, and multiple
configurations that vary by filtration area and type of
inlet/outlet connection. We have a format to meet your
application needs.
OptiScale® Process Development Screening Tool
OptiScale® disposable capsule filters provide a convenient small volume option for
process screening and scaling. These “drop in” filters are ideal for evaluating biopharmaceuticals. OptiScale® capsule filters offer speed-to-market strategies for efficiently
developing compounds and biotherapeutics.
The OptiScale® disposable capsule is ideally suited for process development and
screening. OptiScale® capsules are faster and easier to set up than conventional 25
mm and 47 mm discs.
OptiScale® Filters
Millipak® Low-Volume Capsule Filters
Millipak® filters with hydrophilic Durapore® membranes are uniquely designed for the
removal of particles and microorganisms. The stacked disc design allows minimal holdup volume and no particle shedding, making Millipak® units ideally suited for high
value-added applications such as sterile finish and fill. Each Millipak® filter is integrity
tested during the manufacturing process.
Millipak® Filters
Millipak® filters are available in two different stack sizes. Adjustable, easy-to-turn, upstream vents and drain valves with hose barb connections allow for easy process control.
Cartridge Filters
Hydrophilic Durapore® cartridge filters provide high throughput with minimal differential pressure. Cartridges are robust, strong, resilient and are designed to withstand
multiple steam-in-place cycles. Each Durapore® cartridge filter is integrity tested during the manufacturing process.
A full range of filtration areas is available to suit varying application requirements
and a variety of connection options are offered to meet your application and housing
requirements.
Cartridge Filters
Opticap® XL and XLT Disposable Capsule Filters
Convenient and Easy to Use
Opticap® XL and XLT capsule filters eliminate the time and expense associated with
assembling, cleaning, and validating stainless steel housings. Adjustable, easy-to-turn,
upstream vents and drain valve with O-ring seals and hose barb connections allow
for easy process control. Other ease-of-use features include flow direction arrows and
ribbed housing for easy gripping even with gloved hands.
The Right Size
A wide range of filtration areas is available to fit all of your application needs and to allow
easy scale-up of your small volume filtration steps to larger, full-scale filtration processes.
The Right Connections
Self-contained and disposable, Opticap® XL and XLT capsule filters are supplied with a
choice of inlet and outlet connections to optimize your filtration process, including sanitary flanges which provide a high flow rate, fractional sanitary flanges and hose barbs.
Proven Integrity
Each capsule is integrity tested during the manufacturing process to ensure reliable
performance in your process.
Opticap® XL Filters
Robust Construction
Opticap® XL and XLT capsule design allows unparalleled thermal and hydraulic stress
resistance in a disposable filter, resulting in reliability, high confidence in the sterilization process, and improved cleanliness.
Opticap® XL 2, 4, 5 and 10 Capsule Filters
Opticap® XL disposable capsule filters with hydrophilic Durapore® membrane are
available in multiple filtration areas, providing an optimal choice for every application.
The unique capsule design minimizes hold-up volume and reduces production losses.
Opticap® XLT 10, 20 and 30 Capsule Filters
Opticap® XLT disposable T-line capsule filters with hydrophilic Durapore® membrane
are available with or without a pressure gauge port for ease in monitoring process
conditions. The T-line design accommodates series or parallel filtration to match your
application needs, and a specially-designed stand enables quick and easy integration
into your existing process.
Opticap® XLT Filters
Opticap® XLT Capsule Filter Stand
Specifications
OptiScale® 25 Filters
OptiScale® 47 Filters
Millipak® 100 Filters
Millipak® 200 Filters
Maximum length:
39 mm (1.52 in.) with female
Luer-Lok™ inlet/ male luer
slip outlet
82 mm (3.24 in.) with flange inlet/
hose barb outlet;
74 mm (2.91 in.) with flange inlet/
flange outlet;
94 mm (3.70 in.) with hose barb
inlet/hose barb outlet
13 cm (5.1 in.)
15.5 cm (6.1 in.)
Body diameter:
31 mm (1.21 in.)
70 mm (2.75 in.)
7.6 cm (3.0 in.)
7.6 cm (3.0 in.)
Weight:
0.19 oz (5.5 g)
2.4 oz (69 g)
—
—
3.5 cm2
17.7 cm2
500 cm2 (0.54 ft2)
1000 cm2 (1.08 ft2)
Filter membrane:
Hydrophilic PVDF
Hydrophilic PVDF
Hydrophilic PVDF
Structural components:
Polypropylene
Polycarbonate
Polycarbonate
Supports (when used):
Polypropylene
Polypropylene
—
Vent caps:
Polypropylene
PVDF
PVDF
Internal seal rings:
—
Fluoroelastomers
—
Housing Vent
Capped vent with female Luer
connections on inlet side of
device.
Adjustable vent with male Luer slip and female Luer-Lok™ connections
on inlet side of device.
Maximum Inlet Pressure
4.1 bar (60 psi) at 25 °C
5.5 bar (80 psi) at 25 °C
5.2 bar (75 psi) at 25 °C
Forward:
4.1 bar (60 psi) at 25 °C
5.5 bar (80 psi) at 25 °C
4.1 bar (60 psi) at 25°C
Reverse:
0 psi at 25 °C
0.7 bar (10 psi) at 25 °C
0.7 bar (10 psi) at 25 °C
0.1 µm:
—
—
≥ 4830 mbar (70.0 psig) air with water
0.22 µm:
Nominal Dimensions
Filtration Area
Materials of Construction
Maximum Differential Pressure
Bubble Point at 23 °C
—
—
≥ 3450 mbar (50.0 psig) air with water
NVR Gravimetric Extractables
—
—
After autoclaving and a 24 hour soak in ASTM®
Type 1 reagent grade water at controlled room
temperature:
Oxidizable Substances
—
Meets the requirements of USP Oxidizable Substances Test after a water flush of:
100 mL
200 mL
Bacterial Endotoxin
Aqueous extraction contains
<0.25 EU/mL as determined
by the Limulus Amebocyte
Lysate (LAL) Test.
—
Aqueous extraction contains < 0.5 EU/mL as determined by
the Limulus Amebocyte Lysate (LAL) Test.
Bacterial Retention
—
—
Quantitative retention of 107 CFU/cm2 Brevundimonas
diminuta ATCC® 19146 per ASTM® methodology.
TOC Conductivity
Device effluent met the TOC
acceptance criteria per USP
<643> and the conductivity
acceptance criteria per USP
<645> after autoclaving with a
WFI water flush of 15 mL
—
—
Sterilization
May be autoclaved for 1 cycle
of 60 minutes at 123 °C.
May be autoclaved for 3 cycles of 60
minutes at 126 °C.
May be autoclaved for 3 cycles of 90 minutes at 123 °C.
Capable of 45 kilogray (4.5 Megarad) gamma exposure.
(Cannot be steam sterilized in-line.)
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manfacturing Practices.
Non-Fiber Releasing
Durapore® membrane meets the criteria for a “non-fiber releasing” filter; defined in 21 CFR 210.3 (b) (6).
Component Material Toxicity
Component materials were tested and meet the criteria of the USP <88> Reactivity Test for Class VI Plastics.
Sterilizing-grade Durapore® filters meet the requirements of the current USP <88> Safety Test.
Indirect food additive
The Durapore® membrane used in these products meets the FDA Indirect Food Additive requirements cited in 21 CFR 177.2910.
All other component materials also meet the FDA Indirect Food Additive requirements cited in 21 CFR 177–182.
≤ 2.5 mg
4
≤ 5.0 mg
200 mL
Specifications (continued)
Opticap® XL 2 Filters
Opticap® XL 4 Filters
Opticap® XL 5 Filters
Opticap® XL 10 Filters
Maximum length:
14.2 cm (5.6 in.)
19.6 cm (7.7 in.)
21.6 cm (8.5 in.)
33.5 cm (13.2 in.)
Body diameter:
8.4 cm (3.3 in.)
8.4 cm (3.3 in.)
10.7 cm (4.2 in.)
10.7 cm (4.2 in.)
0.34 m²(3.7 ft )
0.69 m2 (7.4 ft2)
Nominal Dimensions
Filtration Area
0.09 m (0.93 ft )
2
2
0.19 m (2.09 ft )
2
2
2
Materials of Construction
Filter membrane:
Hydrophilic PVDF
Film edge:
Polypropylene
Supports:
Polypropylene
Structural components*:
Polypropylene
Vent O-rings:
Silicone
Vent/Drain
¼ in. hose barb with double O-ring seal
Maximum Inlet Pressure
5.5 bar (80 psi) at 23 °C
2.8 bar (40 psi) at 60 °C
1.0 bar (15 psi) at 80 °C
Maximum Differential Pressure
Forward:
5.5 bar (80 psid) at 25 °C, 1.0 bar (15 psid) at 80 °C
Reverse:
3.4 bar (50 psid) at 25 °C, intermittent
Bubble Point at 23 °C
0.1 µm:
≥ 4830 mbar (70.0 psig) air with water
0.22 µm:
≥ 3450 mbar (50.0 psig) air with water
Air Diffusion
Through a water wet membrane at ambient temperature:
0.1 µm at 3.9 bar (56 psig):
—
≤ 7.5 cc/min
≤ 10.0 cc/min
≤ 20.0 cc/min
0.22 µm of 2.8 bar (40 psig):
—
≤ 5.5 cc/min
≤ 6.6 cc/min
≤ 13.3 cc/min
NVR Gravimetric Extractables
After autoclaving and a 24 hour soak in ASTM® Type 1 reagent grade water at controlled room temperature:
≤ 10 mg
Oxidizable Substances
≤ 10 mg
≤ 15 mg
≤ 25 mg
Meets the requirements of the USP Oxidizable Substances Test after a water flush of:
500 mL
500 mL
500 mL
1000 mL
Bacterial Endotoxin
Aqueous extraction contains < 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test.
Bacterial Retention
Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per ASTM® methodology.
Sterilization
May be autoclaved for 3 cycles of 60 minutes at 126 °C. (Cannot be steam sterilized in-line.)
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Non-Fiber Releasing
Durapore® membrane meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).
Component Material Toxicity
Component materials were tested and meet the criteria of the USP <88> Reactivity Test for Class VI Plastics.
Sterilizing-grade Durapore® filters meet the requirements of the current USP <88> Safety Test.
Indirect Food Additive
The Durapore® membrane used in these products meets the FDA Indirect Food Additive requirements cited in 21 CFR 177.2910.
All other component materials also meet the FDA Indirect Food Additive requirements cited in 21 CFR 177–182.
5
Specifications (continued)
Opticap® XLT 10 Filters
Opticap® XLT 20 Filters
Opticap® XLT 30 Filters
38.1 cm (15.0 in)
62.5 cm (24.6 in.)
87.1 cm (34.3 in.)
Sanitary flange to sanitary flange:
15.2 cm (6.0 in.)
15.2 cm (6.0 in.)
15.2 cm (6.0 in.)
Sanitary flange to hose barb:
17.5 cm (6.9 in.)
17.5 cm (6.9 in.)
17.5 cm (6.9 in.)
Hose barb to hose barb:
19.8 cm (7.8 in.)
19.8 cm (7.8 in.)
19.8 cm (7.8 in.)
0.69 m (7.4 ft )
1.4 m (14.8 ft )
2.1 m2 (22.2 ft2)
Nominal Dimensions
Maximum length:
Fitting to Fitting
Filtration Area
2
2
2
2
Materials of Construction
Filter membrane:
Hydrophilic PVDF
Film edge:
Polypropylene
Supports:
Polypropylene
Structural components*:
Polypropylene
Vent O-rings:
Silicone
Maximum Inlet Pressure
5.5 bar (80 psi) at 23 °C
2.8 bar (40 psi) at 60 °C
1.0 bar (15 psi) at 80 °C
Maximum Differential Pressure
Forward:
5.5 bar (80 psid) at 25 °C, 1.7 bar (25 psid) at 80 °C
Reverse:
3.4 bar (50 psid) at 25°C
Bubble Point at 23 °C
0.1 µm:
≥ 4830 mbar (70.0 psig) air with water
0.22 µm:
≥ 3450 mbar (50.0 psig) air with water
Air Diffusion
Through a water wet membrane at ambient temperature:
0.1 µm at 3.9 bar (56 psig):
≤ 20.0 cc/min
≤ 40.0 cc/min
≤ 60.0 cc/min
0.22 µm of 2.8 bar (40 psig):
≤ 13.3 cc/min
≤ 26.6 cc/min
≤ 39.9 cc/min
NVR Gravimetric Extractables
After autoclaving and a 24 hour soak in ASTM® Type 1 reagent grade water at controlled room temperature:
≤ 25 mg
Oxidizable Substances
≤ 75 mg
Meets the requirements of the USP Oxidizable Substances Test after a water flush of:
1000 mL
2000 mL
3000 mL
Bacterial Endotoxin
Aqueous extraction contains < 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test.
Bacterial Retention
Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per ASTM® methodology.
Sterilization
May be autoclaved for 3 cycles of 60 minutes at 126 °C. (Cannot be steam sterilized in-line.)
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Non-Fiber Releasing
Durapore® membrane meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).
Component Material Toxicity
Component materials were tested and meet the criteria of the USP <88> Reactivity Test for Class VI Plastics.
Sterilizing-grade Durapore® filters meet the requirements of the current USP <88> Safety Test.
Indirect Food Additive
The Durapore® membrane used in these products meets the FDA Indirect Food Additive requirements cited in 21 CFR
177.2910. All other component materials also meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
*Cage, core, end caps and capsule housing
6
≤ 50 mg
Specifications (continued)
5-inch Cartridge
Per 10-inch Cartridge
6.9 cm (2.7 in.)
6.9 cm (2.7 in.)
0.35 m (3.8 ft²)
0.69 m2 (7.4 ft2)
Nominal Dimensions
Outside diameter:
Filtration Area
2
Materials of Construction
Filter membrane:
Hydrophilic PVDF
Film edge:
Polypropylene
Supports:
Polypropylene
Structural components:
Polypropylene
O-rings:
Silicone
Maximum Differential Pressure
Forward:
5.5 bar (80 psid) at 25 °C, 1.7 bar (25 psid) at 80 °C, 345 mbar (5 psid) at 135 °C
Reverse:
3.4 bar (50 psid) at 25 °C, intermittent
Bubble Point at 23 °C
0.1 µm:
≥ 4830 mbar (70.0 psig) air with water
0.22 µm:
≥ 3450 mbar (50.0 psig) air with water
Air Diffusion
0.1 µm at 3.9 bar (56 psig):
0.22 µm of 2.8 bar (40 psig):
NVR Gravimetric Extractables
Through a water wet membrane at ambient temperature:
≤ 10 cc/min
≤ 20.0 cc/min
≤ 6.6 cc/min
≤ 13.3 cc/min
After autoclaving and a 24 hour soak in ASTM® Type 1 reagent grade water at controlled room temperature:
≤ 10 mg
≤ 20 mg
Oxidizable Substances
Meets the requirements of the USP Oxidizable Substances Test after a water flush of:
≤1000 mL per 10-inch element
Bacterial Endotoxin
Aqueous extraction contains < 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test.
Bacterial Retention
Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per ASTM® methodology.
Sterilization
May be autoclaved for 30 cycles of 60 minutes at 126 °C or steam sterilized up to
30 times for 30 minutes at 135 °C.
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Non-Fiber Releasing
Durapore® membrane meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).
Component Material Toxicity
Component materials were tested and meet the criteria of the USP <88> Reactivity Test for Class VI Plastics.
Sterilizing-grade Durapore® filters meet the requirements of the current USP <88> Safety Test.
Indirect Food Additive
The Durapore® membrane used in these products meets the FDA Indirect Food Additive requirements cited
in 21 CFR 177.2910. All other component materials also meet the FDA Indirect Food Additive requirements
cited in 21 CFR 177–182. All component materials meet the requirements of the EU framework regulation
[1935/2004/EC] regarding materials and articles intended to contact food.
Total Organic Carbon (TOC)
and Conductivity
0.1 µm:
Device effluent met the TOC acceptance criteria per USP <643> and the conductivity acceptance
criteria per USP <645> after autoclaving with a WFI water flush of 3.5 L per ten-inch cartridge.
0.22 µm:
Device effluent met the TOC acceptance criteria per USP <643> and the conductivity acceptance
criteria per USP <645> after autoclaving with a WFI water flush of 5.5 L per ten-inch cartridge.
7
Typical Clean Water Flow Rates
Millipak® Capsule Filters
Millipak® 100/200 Capsule Filters —
0.1 µm Hydrophilic Durapore® Membrane
Millipak® 100/200 Capsule Filters —
0.22 µm Hydrophilic Durapore® Membrane
HQN
HQN
1SFTTVSF%SPQCBS
.JMMJQBL
.JMMJQBL
'MPX3BUF-NJO
Opticap® XL 2 Capsule Filters —
0.1 µm Hydrophilic Durapore® Membrane
HQN
QTJ E
HQN
55
''
))
5)
')
'MPX3BUF-NJO
Opticap®0QUJDBQ9-$BQTVMFXJUI%VSBQPSF.FNCSBOF
XL 4 Capsule
Filters —
uN/PNJOBM,77- 0.22 µm Hydrophilic Durapore® Membrane
Opticap® XL 5 Capsule Filters —
0.1 µm Hydrophilic Durapore® Membrane
HQN
HQN
55
''
))
5)
55
''
))
5)
'MPX3BUF-NJO
'MPX3BUF-NJO
'MPX3BUF-NJO
0QUJDBQ9-$BQTVMF'JMUFS
uN)ZESPQIJMJD%VSBQPSF.FNCSBOF,77-
1SFTTVSF%SPQCBS
1SFTTVSF%SPQCBS
55
''
))
5)
Opticap® XL 10 Capsule Filters —
0.22 µm Hydrophilic Durapore® Membrane
QTJE
0QUJDBQ9-$BQTVMF'JMUFS
uN)ZESPQIJMJD%VSBQPSF.FNCSBOF,77-
Opticap® XL 10 Capsule Filters —
0.1 µm Hydrophilic Durapore® Membrane
55
''
))
5)
')
HQN
'MPX3BUF-NJO
0QUJDBQ9-$BQTVMFXJUI%VSBQPSF.FNCSBOF
uN,7(- HQN
Opticap®0QUJDBQ9-$BQTVMFXJUI%VSBQPSF.FNCSBOF
XL 5 Capsule Filters —
uN,77- 0.22 µm Hydrophilic Durapore® Membrane
'MPX3BUF-NJO
'MPX3BUF-NJO
55
''
))
5)
1SFTTVSF%SPQCBS
55
''
))
5)
')
1SFTTVSF%SPQCBS
QTJ E
'MPX3BUF-NJO
HQN
8
Opticap® XL 4 Capsule Filters —
0.1 µm Hydrophilic Durapore® Membrane
55
''
))
5)
')
1SFTTVSF%SPQCBS
Opticap® XL 2 Capsule Filters —
0.22 μm Hydrophilic Durapore® Membrane
1SFTTVSF%SPQCBS
HQN
.JMMJQBL$BQTVMF'JMUFS
uN)ZESPQIJMJD%VSBQPSF.FNCSBOF.1(-
.JMMJQBL$BQTVMF'JMUFS
'MPX3BUF-NJO
uN)ZESPQIJMJD%VSBQPSF.FNCSBOF.17-
Opticap®
XL Capsule Filters
QTJ E
A = 14 mm (9/16 in.) Hose Barb
Inlet and Outlet
B = 6 mm (¼ in.) NPTM Inlet and
Outlet
F = 1 9 mm (¾ in.) Sanitary Flange
Inlet and Outlet
L = 3 8 mm (1½ in.) Sanitary Flange
Inlet and Outlet
0QUJDBQ9-$BQTVMF'JMUFS
uN)ZESPQIJMJD%VSBQPSF.FNCSBOF,7(-
0QUJDBQ9-$BQTVMF'JMUFS
uN)ZESPQIJMJD%VSBQPSF.FNCSBOF,7(-
Opticap® XL Capsule Legends Refer
to Connection Type
TT = 3 8 mm (1½ in.) Sanitary Flange
Inlet and Outlet
FF = 19 mm (¾ in.) Sanitary Flange
Inlet and Outlet
HH = 1 4 mm (9/16 in.) Hose Barb Inlet
and Outlet
TH = 38 mm (1½ in.) Sanitary Flange
Inlet and 14 mm (9/16 in.) Hose
Barb Outlet
FH = 1 9 mm (¾ in.) Sanitary Flange
Inlet and 14 mm (9/16 in.) Hose
Barb Outlet (XL 2 and 4 only)
QTJ E
1SFTTVSF%SPQCBS
1SFTTVSF%SPQCBS
QTJ E
1SFTTVSF%SPQCBS
.JMMJQBL
.JMMJQBL"
.JMMJQBL#
.JMMJQBL'
.JMMJQBL-
QTJ E
QTJ E
QTJE
QTJE
Typical Clean Water Flow Rates
Opticap® XLT Capsule Filters
Opticap® XLT 10 Capsule Filters —
0.1 µm Hydrophilic Durapore® Membrane
HQN
5 5 ##
5)
))
1SFTTVSF%SPQCBS
QTJE
QTJE
0QUJDBQ9- 5XJUI%VSBQPSF.FNCSBOF
Opticap® XLT Capsule Legends Refer to
Connection Type
55
5)
))
##
TT = 38 mm (1½ in.) Sanitary
Flange Inlet and Outlet
TH = 3 8 mm (1½ in.) Sanitary
Flange Inlet and 16 mm (5/8 in.)
Hose Barb Outlet
HH = 16 mm (5/8 in.) Hose Barb Inlet and Outlet
BB = 25 mm (1 in.) Hose Barb Inlet and Outlet
'MPX3BUF-NJO
'MPX3BUF-NJO
5XJUI%VSBQPSF.FNCSBOF
Cartridge0QUJDBQ9Filters
uN,77- 0QUJDBQ9- 5XJUI%VSBQPSF.FNCSBOF
Cartridge Filters —
0.1 µm Hydrophilic Durapore® Membrane
Cartridge Filters — uN,7(- 0.22 µm Hydrophilic Durapore® Membrane
HQN
JODI$BSUSJEHF
JODI$BSUSJEHF
JODI$BSUSJEHF
JODI$BSUSJEHF
'MPX3BUF-NJO
Nu)ZESPQIJMJD%VSBQPSF$BS
USJEHF$77- 5ZQJDBM$MFBO8 BUFS'MPX3BUF
QTJ E
JODI$BSUSJEHF
JODI$BSUSJEHF
JODI$BSUSJEHF
JODI$BSUSJEHF
QTJ E
1SFTTVSF%SPQCBS
HQN
1SFTTVSF%SPQCBS
HQN
Opticap® XLT 30 Capsule Filters —
0QUJDBQ9- 5XJUI%VSBQPSF.FNCSBOF
0.22 µm Hydrophilic
Durapore® Membrane
uN,7(- QTJE
1SFTTVSF%SPQCBS
55
5)
))
##
55
5)
))
##
1SFTTVSF%SPQCBS
HQN
'MPX3BUF-NJO
uN,77
Opticap® XLT 30 Capsule
Filters
—
0.1 µm Hydrophilic Durapore® Membrane
'MPX3BUF-NJO
HQN
Opticap® XLT 20 Capsule Filters —
0.22 µm Hydrophilic Durapore® Membrane
55
5)
))
##
1SFTTVSF%SPQCBS
0QUJDBQ9- 5XJUI%VSBQPSF.FNCSBOF
uN,7(- 5 5 ##
5)
))
0QUJDBQ9- 5XJUI%VSBQPSF.FNCSBOF
uN,77- 'MPX3BUF-NJO
HQN
'MPX3BUF-NJO
Opticap® XLT 20 Capsule Filters —
0.1 µm Hydrophilic Durapore® Membrane
1SFTTVSF%SPQCBS
1SFTTVSF%SPQCBS
QTJE
QTJE
QTJ E
HQN
Opticap® XLT 10 Capsule Filters —
0.22 µm Hydrophilic Durapore® Membrane
'MPX3BUF-NJO
uN)ZESPQIJMJD%VSBQPSF$BS
USJEHF$7(- 5ZQJDBM$MFBO8 BUFS'MPX3BUF
9
Ordering Information
OptiScale® Capsule Filters
S
V
OptiScale®
Capsule Filter
A
Pore Size
VL = 0.1 µm
GL = 0.22 µm
May be Autoclaved
Membrane
Type
V = Durapore®
Disc Size
25 = 25 mm
47 = 47 mm
Quantity
per Package
3 = 3/pk
6 = 6/pk
Connection Type
HH=6 mm (¼ in.) Hose Barb Inlet and Outlet
FF =19 mm (¾ in.) Sanitary Flange Inlet and Outlet
FH = 19 mm (¾ in.) Sanitary Flange Inlet and
6 mm (¼ in.) Hose Barb Outlet
NB=Female Luer-Lok™ Inlet/Male Luer Slip Outlet
Millipak® Capsule Filters
M
P
3
Millipak® Cartridge Filter Series
10C = Millipak® 100, Non-sterile
20C = Millipak® 200, Non-sterile
Millipak®
Capsule Filter
Membrane Pore Size
VL = Durapore® 0.1 µm
GL = Durapore® 0.22 µm
Quantity
per Package
3 = 3/pk
Connection Type
A = 14 mm (9/16 in.) Hose Barb and Outlet
B = 6 mm (¼ in.) NPTM and Outlet
F = 19 mm (¾ in.) Sanitary Flange Inlet and Outlet
L = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet
Opticap® XL Capsule Filters*
K
V
Opticap® XL
Capsule Filter
Membrane Type
V = Durapore®
10
A
Pore Size
VL = 0.1 µm
GL = 0.22 µm
May be Autoclaved
Capsule Size
02 = Opticap® XL 2
04 = Opticap® XL 4
05 = Opticap® XL 5
10 = Opticap® XL 10
Quantity per Package
1 = 1/pk
(Opticap® XL 5 and 10 filters only)
3 = 3/pk
(Opticap® XL 2 and 4 filters only)
Connection Type
TT = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet
FF = 19 mm (¾ in.) Sanitary Flange Inlet and Outlet
HH = 14 mm (9/16 in.) Hose Barb Inlet and Outlet
TH = 38 mm (1½ in.) Sanitary Flange Inlet and
14 mm (9/16 in.) Hose Barb Outlet
FH = 19 mm (¾ in.) Sanitary Flange Inlet and
14 mm (9/16 in.) Hose Barb Outlet (Opticap® XL 2 and
4 filters only)
NN = 6 mm (¼ in.) NPT Inlet and Outlet (Opticap® XL 2 and
4 filters only, 0.22 um only)
Ordering Information
Opticap® XLT Capsule Filters*
K
V
Opticap® XLT
Capsule Filter
A
1
Gauge Port
T = Without Gauge
Port
Z = With Gauge
Port
May be Autoclaved
Pore Size
VL = 0.1 µm
GL = 0.22 µm
Membrane
Type
V = Durapore®
Connection Type
TT = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet
HH = 16 mm (5/8 in.) Hose Barb Inlet and Outlet
TH = 38 mm (1½ in.) Sanitary Flange Inlet and 16 mm
(5/8 in.) Hose Barb Outlet
BB = 25 mm (1 in.) Hose Barb Inlet and Outlet
Capsule Size
1 = Opticap® XLT 10
2 = Opticap® XLT 20
3 = Opticap® XLT 30
Cartridge Filters
C
Cartridge
Filter
Membrane
Type
V = Durapore®
Quantity
per Package
1 = 1/pk
V
Pore Size
VL = 0.1 µm
GL = 0.22 µm
Cartridge Code
0 = (2-222) O-ring
5 = (2-222) O-ring w/spear
7 = (2-226) O-ring with
locking tab and spear
Discription Standard Opticap® XLT Capsule Filter Stand Qty/pk
1
Packaging Code
Cartridge Length
S01 = 1/pk (5-inch element only)
1 = 10 inch
TP3 = 3/pk (all other elements)
2 = 20 inch
3 = 30 inch
5 = 5 inch
(Code 0 and Code 7 only)
Catalogue no.
XLTSTAND1
*Not all configurations available as standard product.
11
To place an order or receive
technical assistance
In the U.S. and Canada,
call toll-free 1-800-645-5476
For other countries across Europe and the world,
please visit: www.emdmillipore.com/offices
For Technical Service, please visit:
www.emdmillipore.com/techservice
www.emdmillipore.com/offices
EMD Millipore, the M logo, Durapore, Millipak, Opticap, and OptiScale are registered trademarks of Merck KGaA, Darmstadt, Germany.
ISO is a registered trademark of the International Organization for Standardization. ASTM is a registered trademark of
American Society for Testing and Materials. ATCC is a registered trademark of American Type Culture Collection.
Luer-Lok is a trademark of Becton Dickinson and Company. Lit No. DS160EN00 Rev. H 06/2015 DP-SBU-11-04815
© 2015 EMD Millipore Corporation, Billerica, MA, USA. All rights reserved.