| Primary Device ID | 00810040253836 |
| NIH Device Record Key | 3aa9ff29-5f12-4338-9f1b-57a1d6df78fe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REP KIT FOR A-SERIES SCOPE |
| Version Model Number | M A730RK |
| Company DUNS | 824793335 |
| Company Name | GLOBAL SURGICAL CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810040253836 [Primary] |
| EPT | Microscope, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-10-04 |
| Device Publish Date | 2024-09-26 |
| 00810040253836 - REP KIT FOR A-SERIES SCOPE | 2024-10-04 |
| 00810040253836 - REP KIT FOR A-SERIES SCOPE | 2024-10-04 |
| 00810040254581 - LASER FILTER MODULE | 2024-10-04 |
| 00810040255113 - HD CAMERA, 1080P V2, A-SERIES | 2024-10-04 |
| 00810040255342 - CAMERA, 4K, USB POWER | 2024-10-04 |
| 00810040255397 - HD CAMERA, 1080P V2, FOR M725 SYS, INT'L | 2024-10-04 |
| 00810040255403 - LED LIGHT SOURCE, A-SERIES, V2 | 2024-10-04 |
| 00810040255434 - A-SERIES SUPPORT ARM, HORIZONTAL, V2 | 2024-10-04 |
| 00810040255441 - A-SERIES SUPPORT ARM, 45 DEGREE, V2 | 2024-10-04 |