icotec Instrument Implant Holder for Tamping 38-036

GUDID 07640164841830

icotec Instrument Implant Holder for Tamping

icotec AG

Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block Bone graft packing block
Primary Device ID07640164841830
NIH Device Record Key32ee54c3-f613-4bd6-9761-ccf880d0c19b
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Instrument Implant Holder for Tamping
Version Model Number38-036
Catalog Number38-036
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107640164841830 [Primary]

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


[07640164841830]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-09-06
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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