Primary Device ID | 09348215123857 |
NIH Device Record Key | d08c563f-bd55-4d61-a394-9921448b675f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rx Knee All Poly Tibia Augment - Third |
Version Model Number | 121-20-9335 |
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 | 09348215123857 [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 | 2024-11-20 |
Device Publish Date | 2024-11-12 |
09348215123987 | 121-20-9329 |
09348215123970 | 121-20-9328 |
09348215123963 | 121-20-9327 |
09348215123956 | 121-20-9326 |
09348215123949 | 121-20-9325 |
09348215123932 | 121-20-9324 |
09348215123925 | 121-20-9323 |
09348215123918 | 121-20-9322 |
09348215123901 | 121-20-9321 |
09348215123895 | 121-20-9339 |
09348215123888 | 121-20-9338 |
09348215123871 | 121-20-9337 |
09348215123864 | 121-20-9336 |
09348215123857 | 121-20-9335 |
09348215123840 | 121-20-9334 |
09348215123833 | 121-20-9333 |
09348215123826 | 121-20-9332 |
09348215123819 | 121-20-9331 |