| Primary Device ID | 09348215066239 |
| NIH Device Record Key | 5a7c2eef-be3b-402f-b9e6-ff6984bfad73 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | XM Shaft Single End Trial |
| Version Model Number | 132-25-0021 |
| 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 | 09348215066239 [Primary] |
| HWT | Template |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
[09348215066239]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-03 |
| Device Publish Date | 2020-06-25 |