AXE D'ANTEVERSION POUR IMPACTEUR DE COTYLE

GUDID 03661489415043

FOURNITURES HOSPITALIERES INDUSTRIE

Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID03661489415043
NIH Device Record Keyf9e1f570-510f-43a2-a93a-e85352e1b30d
Commercial Distribution StatusIn Commercial Distribution
Brand NameAXE D'ANTEVERSION POUR IMPACTEUR DE COTYLE
Version Model Number241504
Company DUNS261839898
Company NameFOURNITURES HOSPITALIERES INDUSTRIE
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS103661489415043 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


[03661489415043]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-05-03
Device Publish Date2019-03-13