| Primary Device ID | 04059082010342 |
| NIH Device Record Key | 6997a4f8-8b96-4870-897e-718f28efd49a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cystoscopy adaptor |
| Version Model Number | 196 800 150BC |
| 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 | 04059082010342 [Primary] |
| FAJ | Cystoscope and accessories, flexible/rigid |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04059082010342]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-12-22 |
| 04059082030654 | 198 050 300 |
| 04059082030647 | 198 050 200 |
| 04059082030630 | 198 050 100 |
| 04059082030500 | 196 810 150 |
| 04059082030494 | 196 810 111 |
| 04059082030470 | 196 800 150 |
| 04059082030319 | 196 050 300 |
| 04059082030302 | 196 050 200 |
| 04059082030296 | 196 050 100 |
| 04059082010588 | 198 050 300BC |
| 04059082010571 | 198 050 200BC |
| 04059082010564 | 198 050 100BC |
| 04059082010397 | 196 810 150BC |
| 04059082010380 | 196 810 111BC |
| 04059082010342 | 196 800 150BC |
| 04059082010144 | 196 050 300BC |
| 04059082010137 | 196 050 200BC |
| 04059082010120 | 196 050 100BC |