| Primary Device ID | 09348215039783 |
| NIH Device Record Key | 6884394d-6385-49b1-8a1d-17a69e1adcea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Origin Broach |
| Version Model Number | 111-18-1809 |
| 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 | 09348215039783 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[09348215039783]
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 |
| 09348215039783 | 111-18-1809 |
| 09348215039776 | 111-18-1609 |
| 09348215039769 | 111-18-1509 |
| 09348215039752 | 111-18-1409 |
| 09348215039745 | 111-18-1309 |
| 09348215039738 | 111-18-1209 |
| 09348215039721 | 111-18-1109 |
| 09348215039714 | 111-18-1009 |
| 09348215039707 | 111-18-0909 |
| 09348215039691 | 111-18-0809 |
| 09348215039684 | 111-18-0609 |