| Primary Device ID | 00810041631831 |
| NIH Device Record Key | 36b36a77-3fd3-49b0-a0c5-d97cfb29dc96 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Smith and Nephew |
| Version Model Number | 7205324 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| 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 | 00810041631831 [Primary] |
| GS1 | 10810041631838 [Package] Package: Box [6 Units] In Commercial Distribution |
| GS1 | 20810041631835 [Package] Contains: 10810041631838 Package: Case [24 Units] In Commercial Distribution |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-08-25 |
| Device Publish Date | 2019-12-13 |