icotec Instrument Inserter Sleeve with Depth Limiter 41-13-3

GUDID 07640164842363

icotec Instrument Inserter Sleeve with Depth Limiter

icotec AG

Orthopaedic implant inserter/extractor, reusable
Primary Device ID07640164842363
NIH Device Record Keyeab2572d-e57e-49e0-b1e4-82276d7ec607
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Instrument Inserter Sleeve with Depth Limiter
Version Model Number41-13-3
Catalog Number41-13-3
Company DUNS480789465
Company Nameicotec AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch

Device Identifiers

Device Issuing AgencyDevice ID
GS107640164842363 [Primary]

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

[07640164842363]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-04-23
Device Publish Date2018-07-16

Devices Manufactured by icotec AG

07640172553916 - KONG-TL VBR System, Guiding Sleeve for locking screwdriver2026-02-06 KONG-TL VBR System, Guiding Sleeve for locking screwdriver
07640172552544 - CMORE® System, Awl2025-12-02 CMORE® System, Awl
07640172552551 - CMORE® System, Pedicle Probe, Straight2025-12-02 CMORE® System, Pedicle Probe, Straight
07640172552568 - CMORE® System, Drill Guide Sleeve2025-12-02 CMORE® System, Drill Guide Sleeve
07640172552575 - CMORE® System, Drill Guide Stop2025-12-02 CMORE® System, Drill Guide Stop
07640172552582 - CMORE® System, Drill Bit, Ø 2.3 mm2025-12-02 CMORE® System, Drill Bit, Ø 2.3 mm
07640172552599 - CMORE® System, Feeler2025-12-02 CMORE® System, Feeler
07640172552605 - CMORE® System, In-line Handle, AO Coupling2025-12-02 CMORE® System, In-line Handle, AO Coupling
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