icotec Instrument Rasp 38-037

GUDID 07640164841847

icotec Instrument Rasp

icotec AG

Bone file/rasp, manual Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable
Primary Device ID07640164841847
NIH Device Record Key6cf0ab43-dd80-445a-8302-687f6413dc1d
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Instrument Rasp
Version Model Number38-037
Catalog Number38-037
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107640164841847 [Primary]

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


[07640164841847]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-12-07
Device Publish Date2018-07-16

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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

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