EIT CIF Impactor

GUDID 04260397080221

Impactor

EIT Emerging Implant Technologies GmbH

Orthopaedic implant impactor
Primary Device ID04260397080221
NIH Device Record Keycf895472-fa9c-4134-97fc-581d33d87eaf
Commercial Distribution StatusIn Commercial Distribution
Brand NameEIT CIF Impactor
Version Model NumberCET30201
Company DUNS313088331
Company NameEIT Emerging Implant Technologies GmbH
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104260397080221 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ODPIntervertebral Fusion Device With Bone Graft, Cervical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04260397080221]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-12-11
Device Publish Date2018-01-05

On-Brand Devices [EIT CIF Impactor]

04260397081044Impactor without depth stop
04260397080221Impactor

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