| Primary Device ID | 05060548211271 |
| NIH Device Record Key | 5d1eb619-666d-45aa-979e-b05fa36b3953 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Versius Fenestrated Grasper |
| Version Model Number | 10320 |
| Company DUNS | 219860797 |
| Company Name | CMR SURGICAL LIMITED |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05060548211271 [Primary] |
| SCV | Modular Electromechanical Surgical System |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[05060548211271]
Ethylene Oxide
[05060548211271]
Ethylene Oxide
[05060548211271]
Ethylene Oxide
[05060548211271]
Ethylene Oxide
[05060548211271]
Ethylene Oxide
[05060548211271]
Ethylene Oxide
[05060548211271]
Ethylene Oxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-03-17 |
| Device Publish Date | 2026-03-09 |