| Primary Device ID | 04059082026640 |
| NIH Device Record Key | 9d2d7710-0901-41ec-9f90-c111905490ee |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Monopolar HF cable |
| Version Model Number | 395 502 501 |
| 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 | 04059082026640 [Primary] |
| FAS | ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04059082026640]
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 |
| 04059082026718 | 395 502 508 |
| 04059082026701 | 395 502 507 |
| 04059082026695 | 395 502 506 |
| 04059082026688 | 395 502 505 |
| 04059082026671 | 395 502 504 |
| 04059082026664 | 395 502 503 |
| 04059082026657 | 395 502 502 |
| 04059082026640 | 395 502 501 |
| 04059082026633 | 395 502 500 |
| 04059082009421 | 195 200 004 |
| 04059082009414 | 195 200 003 |
| 04059082009407 | 195 200 002 |
| 04059082009391 | 195 200 001 |