| Primary Device ID | 09348215040291 |
| NIH Device Record Key | c40c0245-a185-4dce-9f9c-c5a2ff3274f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Aria Broach |
| Version Model Number | 111-20-6210 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 09348215040291 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[09348215040291]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-04 |
| Device Publish Date | 2018-10-02 |
| 09348215040314 | 111-20-6212 |
| 09348215040307 | 111-20-6211 |
| 09348215040291 | 111-20-6210 |
| 09348215040284 | 111-20-6209 |
| 09348215040277 | 111-20-6208 |
| 09348215040260 | 111-20-6207 |
| 09348215040253 | 111-20-6206 |
| 09348215040246 | 111-20-6205 |
| 09348215040239 | 111-20-6204 |
| 09348215040222 | 111-20-6203 |
| 09348215040215 | 111-20-6202 |
| 09348215040208 | 111-20-6201 |
| 09348215040192 | 111-20-6200 |