icotec Anterior Cervical Plate System, Cervical Plate, Container, complete 39-11

GUDID 07640140434599

icotec Anterior Cervical Plate System, Cervical Plate, Container, complete

icotec AG

Device sterilization/disinfection container, reusable
Primary Device ID07640140434599
NIH Device Record Key44214586-5aa1-485c-9c1e-022ed3445dec
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Anterior Cervical Plate System, Cervical Plate, Container, complete
Version Model Number39-11
Catalog Number39-11
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107640140434599 [Primary]

FDA Product Code

KWQAppliance, Fixation, Spinal Intervertebral Body

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

[07640140434599]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-18
Device Publish Date2023-09-08

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