Primary Device ID | 09348215116439 |
NIH Device Record Key | 63b232c1-29a5-471c-86a0-a257e299f149 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | World Knee UC All Poly Tibia |
Version Model Number | 121-20-6139 |
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 | 09348215116439 [Primary] |
JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-07 |
Device Publish Date | 2023-07-28 |
09348215116170 | 121-20-6238 |
09348215116163 | 121-20-6138 |
09348215116514 | 121-20-6939 |
09348215116507 | 121-20-6839 |
09348215116491 | 121-20-6739 |
09348215116484 | 121-20-6639 |
09348215116477 | 121-20-6539 |
09348215116460 | 121-20-6439 |
09348215116453 | 121-20-6339 |
09348215116446 | 121-20-6239 |
09348215116439 | 121-20-6139 |
09348215116248 | 121-20-6938 |
09348215116231 | 121-20-6838 |
09348215116224 | 121-20-6738 |
09348215116217 | 121-20-6638 |
09348215116200 | 121-20-6538 |
09348215116194 | 121-20-6438 |
09348215116187 | 121-20-6338 |