| Primary Device ID | 04059082031651 |
| NIH Device Record Key | 4ec6f7ed-8e04-44de-bc84-5f524b24fc36 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Resectoscopy working element |
| Version Model Number | 199 020 000 |
| 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 | 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 | 04059082031651 [Primary] |
| FDC | RESECTOSCOPE, WORKING ELEMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04059082031651]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-03-11 |
| Device Publish Date | 2018-03-20 |
| 04059082031651 | 199 020 000 |
| 04059082031644 | 199 010 020 |
| 04059082031606 | 195 810 000 |
| 04059082031576 | 195 800 000 |
| 04059082031545 | 195 400 000 |
| 04059082031293 | 195 020 050 |
| 04059082031286 | 195 020 040 |
| 04059082031279 | 195 020 000 |
| 04059082031262 | 195 010 040 |
| 04059082031255 | 195 010 000 |
| 04059082025391 | 395 015 002 |
| 04059082025384 | 395 015 001 |
| 04059082010687 | 199 020 000BC |
| 04059082010656 | 199 010 020BC |
| 04059082009780 | 195 810 000BC |
| 04059082009599 | 195 800 000BC |
| 04059082009506 | 195 400 000BC |
| 04059082008479 | 195 020 050BC |
| 04059082008462 | 195 020 040BC |
| 04059082008431 | 195 020 000BC |
| 04059082008400 | 195 010 040BC |
| 04059082008370 | 195 010 000BC |