Primary Device ID | 09348215115982 |
NIH Device Record Key | 16c2aa85-2871-4873-9e3b-764bc360957c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | World Knee CR All Poly Tibia |
Version Model Number | 121-20-6118 |
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 | 09348215115982 [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 |
09348215116255 | 121-20-6119 |
09348215116330 | 121-20-6919 |
09348215116323 | 121-20-6819 |
09348215116316 | 121-20-6719 |
09348215116309 | 121-20-6619 |
09348215116293 | 121-20-6519 |
09348215116286 | 121-20-6419 |
09348215116279 | 121-20-6319 |
09348215116262 | 121-20-6219 |
09348215116064 | 121-20-6918 |
09348215116057 | 121-20-6818 |
09348215116040 | 121-20-6718 |
09348215116033 | 121-20-6618 |
09348215116026 | 121-20-6518 |
09348215116019 | 121-20-6418 |
09348215116002 | 121-20-6318 |
09348215115999 | 121-20-6128 |
09348215115982 | 121-20-6118 |