| Primary Device ID | 04059082007243 |
| NIH Device Record Key | 0d6f620a-5983-4998-9cdc-19d4aca7f3bd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arthroscope Bridge |
| Version Model Number | 191 401 781 |
| Company DUNS | 507185952 |
| Company Name | SOPRO-COMEG GmbH |
| 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 | 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 | 04059082007243 [Primary] |
| HRX | Arthroscope |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04059082007243]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-03-11 |
| Device Publish Date | 2018-04-12 |
| 04059082003559 - Thoracoscope | 2019-11-08 |
| 04059082003757 - Hysteroscope | 2019-11-08 |
| 04059082003764 - Hysteroscope | 2019-11-08 |
| 04059082003795 - Hysteroscope | 2019-11-08 |
| 04059082003818 - Hysteroscope | 2019-11-08 |
| 04059082003856 - Hysteroscope | 2019-11-08 |
| 04059082003870 - Hysteroscope | 2019-11-08 |
| 04059082003894 - Hysteroscope | 2019-11-08 |