Primary Device ID | 09348215087258 |
NIH Device Record Key | f4b6a926-8796-47c8-a7c9-b42cc9a13f40 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Origin NS Stem |
Version Model Number | 111-23-5041 |
Company DUNS | 751993028 |
Company Name | SIGNATURE ORTHOPAEDICS PTY LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09348215087258 [Primary] |
MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-11 |
Device Publish Date | 2021-10-01 |
09348215087289 | 111-23-5052 |
09348215087272 | 111-23-5051 |
09348215087265 | 111-23-5042 |
09348215087258 | 111-23-5041 |
09348215087241 | 111-23-5032 |
09348215087234 | 111-23-5031 |
09348215087227 | 111-23-5022 |
09348215087210 | 111-23-5021 |
09348215087203 | 111-23-5012 |
09348215087197 | 111-23-5011 |
09348215087180 | 111-23-5002 |
09348215087173 | 111-23-5001 |