icotec Instrument Inserter Grip, PLIF 38-028

GUDID 07640164841731

icotec Instrument Inserter Grip, PLIF

icotec AG

Orthopaedic implant inserter/extractor, reusable
Primary Device ID07640164841731
NIH Device Record Key1f3ae1ef-25f8-44b6-b132-21b595c53e18
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Instrument Inserter Grip, PLIF
Version Model Number38-028
Catalog Number38-028
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
GS107640164841731 [Primary]

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

[07640164841731]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-04-23
Device Publish Date2018-07-16

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