Primary Device ID | 09348215029104 |
NIH Device Record Key | fbab51bb-89bb-4a73-8b14-a809be32fca5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bio-composite Screw |
Version Model Number | 121-05-7278 |
Company DUNS | 751993028 |
Company Name | SIGNATURE ORTHOPAEDICS PTY LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | 09348215029104 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-05 |
Device Publish Date | 2023-05-26 |
09348215116705 | 121-05-2379 |
09348215116699 | 121-05-2329 |
09348215116682 | 121-05-1379 |
09348215116675 | 121-05-1329 |
09348215116668 | 121-05-0379 |
09348215116651 | 121-05-0329 |
09348215116644 | 121-05-9379 |
09348215116637 | 121-05-9329 |
09348215116620 | 121-05-9278 |
09348215116613 | 121-05-9279 |
09348215116606 | 121-05-8329 |
09348215116590 | 121-05-8278 |
09348215116583 | 121-05-8279 |
09348215029135 | 121-05-8238 |
09348215029128 | 121-05-8239 |
09348215029111 | 121-05-7329 |
09348215029104 | 121-05-7278 |
09348215122119 | 121-05-7279 |
09348215122102 | 121-05-7238 |
09348215122096 | 121-05-7239 |
09348215122089 | 121-05-6279 |
09348215122072 | 121-05-6238 |
09348215122065 | 121-05-6239 |
09348215122058 | 121-05-5239 |