Primary Device ID | 09348215116415 |
NIH Device Record Key | 5505c1e7-bd2e-4fab-ab83-35b04bdd34ac |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | World Knee PS All Poly Tibia |
Version Model Number | 121-20-6809 |
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 | 09348215116415 [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 | 2023-08-01 |
Device Publish Date | 2023-07-24 |
09348215116422 | 121-20-6909 |
09348215116415 | 121-20-6809 |
09348215116408 | 121-20-6709 |
09348215116392 | 121-20-6609 |
09348215116385 | 121-20-6509 |
09348215116378 | 121-20-6409 |
09348215116125 | 121-20-6608 |
09348215116095 | 121-20-6308 |
09348215116361 | 121-20-6309 |
09348215116354 | 121-20-6209 |
09348215116347 | 121-20-6109 |
09348215116156 | 121-20-6908 |
09348215116149 | 121-20-6808 |
09348215116132 | 121-20-6708 |
09348215116118 | 121-20-6508 |
09348215116101 | 121-20-6408 |
09348215116088 | 121-20-6208 |
09348215116071 | 121-20-6108 |