icotec Instrument, Template for, 4 Segmental Plate 74 mm

GUDID 07640140438719

icotec Instrument, Template for, 4 Segmental Plate 74 mm

icotec AG

Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable
Primary Device ID07640140438719
NIH Device Record Key9bbf9459-e37a-42a4-88e4-b25cd92b2481
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Instrument, Template for, 4 Segmental Plate 74 mm
Version Model Number39-18-4-74
Company DUNS480789465
Company Nameicotec AG
Device Count1
DM Exempttrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107640140438719 [Primary]

FDA Product Code

KWQAppliance, Fixation, Spinal Intervertebral Body

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


[07640140438719]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-15
Device Publish Date2021-01-07

Devices Manufactured by icotec AG

07640172551974 - VADER Pedicle System, Fixation device2024-03-27 VADER Pedicle System, Fixation device
07640140430324 - icotec Lumbar Cage ETurn TLIF 7 x 12 mm2024-03-06 icotec Lumbar Cage ETurn TLIF 7 x 12 mm
07640140430331 - icotec Lumbar Cage ETurn TLIF 9 x 12 mm2024-03-06 icotec Lumbar Cage ETurn TLIF 9 x 12 mm
07640140430348 - icotec Lumbar Cage ETurn TLIF 11 x 12 mm2024-03-06 icotec Lumbar Cage ETurn TLIF 11 x 12 mm
07640140430355 - icotec Lumbar Cage ETurn TLIF 13 x 12 mm2024-03-06 icotec Lumbar Cage ETurn TLIF 13 x 12 mm
07640140430362 - icotec Lumbar Cage ETurn TLIF 15 x 12 mm2024-03-06 icotec Lumbar Cage ETurn TLIF 15 x 12 mm
07640140430379 - icotec Lumbar Cage ETurn TLIF 07 x 16 mm2024-03-06 icotec Lumbar Cage ETurn TLIF 07 x 16 mm
07640140430386 - icotec Lumbar Cage ETurn TLIF 09 x 16 mm2024-03-06 icotec Lumbar Cage ETurn TLIF 09 x 16 mm

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.