| Primary Device ID | 04059082012926 |
| NIH Device Record Key | fd0a1a02-e5d7-497e-9415-fb825db71c93 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bipolar HF cable |
| Version Model Number | 390 813 000 |
| 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 | 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 | 04059082012926 [Primary] |
| FAS | ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04059082012926]
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 | 2016-09-12 |
| 04059082013039 | 390 865 000 |
| 04059082013022 | 390 863 000 |
| 04059082012995 | 390 845 000 |
| 04059082012988 | 390 843 000 |
| 04059082012971 | 390 835 000 |
| 04059082012964 | 390 833 000 |
| 04059082012957 | 390 825 000 |
| 04059082012940 | 390 823 000 |
| 04059082012933 | 390 815 000 |
| 04059082012926 | 390 813 000 |
| 04059082012919 | 390 805 000 |
| 04059082012902 | 390 803 000 |