NP RP WP
NON-TOUCH
Step 1
The non-sterile personnel should open the sealed blister [1] and drop the package and identification labels in a sterile field.
Step 2
Staff must unscrew the sterile package cap [8] and place the container body [2] upright on a flat surface.
Step 3
The surgeon must connect the implant carrier with adapter ratchet wrench or C / A in your choice of manual or motor
placement.
Step 4
Once connected, axial pressure on the implant carrier to retain and remove all non-touch [5 +6 +7] packages.
Step 5
Remove the carrier Non-Touch device gently tilting the set.
CAUTION: It is important not to make sudden movements to avoid unintentional disconnection of the carrier
and the ratchet or wrench adapter C / A.
Book the whole "Support-Non Touch" for later extraction of the healing cap
Step 6
Insert the implant over the surgical area with ratchet or motor as chosen in Step 3.
Step 7
Remove the carrier as outlined in B-0042 [Quick Guide].
Step 8
With the help of hex adapter [Ref 50 08 01 or 50 08 02], and as long as the choice is to perform a two-stage surgery, we
proceed to the extraction of the cover screw of its support. [9] This should fit the hex adapter with the cover screw, by exerting
an axial pressure in order to join the two components together firmly maintaining the "Stand-Non Touch".
list of references
50 37 06
50 37 08
50 37 10
50 37 12
50 37 14
RP KL IMPLANT Ø 3,7 X 06 MM
RP KL IMPLANT Ø 3,7 X 08 MM
RP KL IMPLANT Ø 3,7 X 10 MM
RP KL IMPLANT Ø 3,7 X 12 MM
RP KL IMPLANT Ø 3,7 X 14 MM
50 42 06
50 42 08
50 42 10
50 42 12
50 42 14
RP KL IMPLANT Ø 4,2 X 06 MM
RP KL IMPLANT Ø 4,2 X 08 MM
RP KL IMPLANT Ø 4,2 X 10 MM
RP KL IMPLANT Ø 4,2 X 12 MM
RP KL IMPLANT Ø 4,2 X 14 MM
50 33 08
50 33 10
50 33 12
50 33 14
NP KL IMPLANT Ø 3,3 X 08 MM
NP KL IMPLANT Ø 3,3 X 10 MM
NP KL IMPLANT Ø 3,3 X 12 MM
NP KL IMPLANT Ø 3,3 X 14 MM
50 47 08
50 47 10
50 47 12
50 47 14
WP KL IMPLANT Ø 4,7 x 08 MM
WP KL IMPLANT Ø 4,7 x 10 MM
WP KL IMPLANT Ø 4,7 x 12 MM
WP KL IMPLANT Ø 4,7 x 14 MM
Step 9
Turn in the opposite direction from clockwise to release the cover screw.
Step 10
Remove the cover screw from its bracket.
ATTENTION: It is important not to make sudden movements to avoid unintentional disconnection of the adapter
and healing cap/cover screw
Step 11
Screw the healing cap into the implant.
COLOR CODE
SURGICAL DIAMETER
SHOULDER DIAMETER
YELLOW
3.3 MM
3.5 MM
RED
3.7 MM
4.1 MM
BLUE
4.2 MM*
4.1 MM
GREEN
4.7 MM*
5.1 MM
Color Chart - diameter drills and implants.
*IMPLANTS WITH 4.2 / 4.7 MM DIAMETER ARE NOTSUITABLE FOR BONE TYPE D1, D2.
Step 1
Step 2
Step 3a
Step 4a
SOADCO S. L. IS A MANUFACTURER OF SURGICAL-MEDICAL MATERIAL, SPECIFICALLY DENTAL IMPLANTS AND
RELATED SURGICAL-MEDICAL PRODUCTS. KLOCKNER NORTH AMERICA, INC IS THE OFFICIAL DISTRIBUTOR IN
USA.
SOADCO S. L., KLOCKNER OF NORTH AMERICA AND/OR OTHER OFFICIAL DISTRIBUTORS DO NOT PRACTICE
MEDICINE OR DENTISTRY AND THEREFORE DO NOT RECOMMEND EITHER SURGICAL TECHNIQUES OR DENTALMEDICAL EQUIPMENT FOR PATIENTS.
Step 5a
Step 6a
Step 3b
Step 4b
Step 5b
Step 6b
SOADCO S. L., KLOCKNER OF NORTH AMERICA, INC. AND/OR OTHER OFFICIAL DISTRIBUTORS DO NOT
GUARANTEE A PARTICULAR RESULT OR BENEFITS ARISING FROM THE USE OF SUCH DENTAL-MEDICAL
EQUIPMENT MANUFACTURED AND/OR SOLD BY THEMSELVES, AND DECLINE / REFUSE ANY RESPONSIBILITY
REGARDING THE USE OF THE MATERIAL BASED ON THE INTERPRETATION OF THE INFORMATION DESCRIBED IN
THIS DOCUMENT, BECAUSE A PARTICULAR OUTCOME CANNOT BE GUARANTEED.
ANY WITNESS, OPINION OR INSTRUCTION DESCRIBED IN THIS DOCUMENT AND DISTRIBUTED TO ANY
HEALTHCARE PROFESSIONAL, CLINICIAN, RESEARCHER, OR ANY QUALIFIED PERSONNEL ARE ONLY THEIR
TESTIMONY, OPINIONS, OR INSTRUCTIONS. THESE ARE NOT TESTIMONY, OPINIONS, OR INSTRUCTIONS FROM
EMPLOYEES OF SOADCO S. L., KLOCKNER OF NORTH AMERICA, INC. AND/OR OTHER OFFICIAL DISTRIBUTORS.
THEREFORE, SOADCO S. L., KLOCKNER OF NORTH AMERICA, INC. AND/OR OTHER OFFICIAL DISTRIBUTORS ARE
NOT RESPONSIBLE FOR ANY CLAIM OR STATEMENT MADE BY SUCH PARTIES.
THE PRODUCTS DESCRIBED IN THIS DOCUMENT ARE FOR THEIR ACQUISITION AND USE ONLY BY DENTALMEDICAL PROFESSIONALS APPROPRIATELY TRAINED AND QUALIFIED IN THIS FIELD AND MUST NOT BE
RESOLD.
THE DEVICES DESCRIBED IN THIS DOCUMENT ARE MANUFACTURED BY:
SOADCO, SL
AVGDA. FITER I ROSSELL, 4 BIS LOCAL Nº 2
ESCALDES-ENGORDANY [ANDORRA]
AND DISTRIBUTED IN USA BY:
KLOCKNER OF NORTH AMERICA.
175 SW 7TH STREET, UNIT 1103-1104
MIAMI, FL, 33130 [USA]
THE USE AND/OR SELECTION OF AN INAPPROPRIATE TREATMENT OF ANY MEDICAL AND/OR SURGICAL
MATERIALS DESCRIBED IN THIS DOCUMENT, IS SOLELY RESPONSIBILITY OF THE USER OF SUCH MATERIAL.
WARNING
NOT ALL KLOCKNER ® IMPLANT SYSTEM PRODUCTS ARE AVAILABLE IN ALL COUNTRIES.
Step 8
Step 9
Step 10
Step 11
www.klocknerimplantsystem.com
KL is a threaded implant slightly arched with two sections at the tip to facilitate its surgical insertion, without having to pass
previously the initiator of turns, except for hard bones as D1/D2 where it is essential to pass the corresponding initiator
[as selected diameter]. They feature a double spiral, a step forward in 2.2 mm that reduces surgical time.
KL IMPLANTS
NP
RP
KL implants presented as a hex connection of 0.7 mm high. The connection allows anti rotational hexagonal and
replacement of the attachment and screw through its complete immobilization is achieved.
WP
KL, implant with external connection KLOCKNER ® IMPLANT SYSTEM, has
been specially designed and intended for the treatment of all surgical and
prosthetic solutions.
NP
RP
0.7 MM
· Demanding quality standards [EC, FDA].
· Experience accumulated over 20 years in the market.
Philosophy of KLOCKNER ® IMPLANT SYSTEM:
· Innovation
· Security
· Simplicity
· Aesthetics
WP
M 2.0 MM
2.4 MM
BETWEEN
FACES
Ø 3.5 MM
0.7 MM
M 1.6 MM
M 2.5 MM
0.7 MM
The KLOCKNER ® IMPLANT SYSTEM products are the result of:
2.7 MM
BETWEEN
FACES
3.4 MM
BETWEEN
FACES
Ø 4.1 MM
Ø 5.1 MM
NP KL implant is made of titanium commercially pure grade 4, cold-worked
and with 60% more strength than conventional titanium grade 4. This new
titanium increases the mechanical safety in narrow diameter implants.
PACKAGING
KL implant is provided in a double package
that ensures optimal preservation and
storage while maintaining it sterile. Implant
facilitates manipulation safely to their
insertion over the surgical area.
RP KL and WP KL implants are made of titanium commercially pure grade
3.
Shot Blasting treated for greater surface apposition bone and better
stability and acid passivation layer forming a stable titanium oxide ion
outlet preventing the physiological environment.
9
GENERAL CLINICAL CONSIDERATIONS
All clinical recommendations and warnings described are general
guidelines. The practitioner must his knowledge and judge whether these
general guidelines are appropriate in each case.
Physiological and anatomical conditions may adversely affect the
effectiveness of the dental implants. Some important parameters to
consider when placing dental implants are:
· Poor bone quality.
· Poor oral hygiene.
· Medical conditions.
· Tobacco.
SURFACE TREATMENT
Greater surface contact.
PROGRESSIVE CORE
The apical zone scheduled emerges with a taper that facilitates the placement of the implant.
The central zone of the parallel walls offers a primary stability.
The cervical cone, ending at the maximum diameter of 4.1 mm
from the shoulder of the implant platform.
1·
2·
3·
4·
5·
6·
7·
8·
9·
DOUBLE SPIRAL
Reduces surgical time.
APEX TAPPING
1000
G4 ASTM F67 vs G4 CW
Facilitates the placement of the implant in the bed without passing
the initiator of turns in low-density bone [D3-D4].
Stress [MPa]
800
700
600
500
400
300
Yield strength
Maximum strength
PRODUCT WARNINGS
EXCESSIVE BONE COMPRESSION IN A RECEIVER MAY CAUSE THE NO OSSEOINTEGRATION OF THE IMPLANT
FAILURE TO FOLLOW THE STEPS OUTLINED IN SURGICAL SEQUENCE CAN CAUSE:
· LACK OF STABILITY FOR PRIMARY BONE LOSS SUPPORT.
· DIFFICULTIES IN IMPLANT PLACEMENT.
EXCEED THE TORQUE [45 Ncm] IN THE PLACEMENT OF THE IMPLANT MAY PRODUCE:
· IRREVERSIBLE DISTORTION IN THE EXTERNAL CONNECTION.
· IRREVERSIBLE DEFORMATION IN INSTRUMENTS INDICATED FOR IMPLANT PLACEMENT
· DIFFICULTIES IN THE REMOVAL OF MATERIALS/IMPLANTS
B-00041-EN
REV. 03
x3
x1
* THREE IDENTIFICATION LABELS FOR CLINICAL HISTORY AND A FOURTH
LABEL TO FACILITATE YOUR ORDERS.
WARNINGS
RECEIVED MATERIAL MUST BE PERFECTLY PACKED. OTHERWISE CONTACT YOUR REPRESENTATIVE.
DO NOT USE MATERIAL IF THE PACKAGING IS OPEN, DAMAGED OR HAS EXPIRED.
STERILE MATERIAL, OR MATERIAL INTENDED FOR SINGLE USE, SHOULD NEVER BE REUSED UNDER
ANY CIRCUMSTANCE, SINCE THE OPTIMUM CONDITIONS OF QUALITY AND STERILITY WITH WHICH
THE PRODUCT IS SUPPLIED WOULD BE LOST, AS WELL AS ITS PERFORMANCE.
900
G4 ASTM F67
G4 CW
BLISTER SEALED
PACKAGE BODY
IDENTIFICATION LABELS *
IDENTIFYING COLOR WASHER
NON TOUCH
IMPLANT
CARRIER
PACKAGE CAP
COVER CAP HOLDER
IMAGES MADE BY THE KLOCKNER-UPC, USING
TECHNOLOGY FIB [FOCUSED ION BEAM]