Primary Device ID | 04059082026671 |
NIH Device Record Key | c2b9d026-e70b-4810-9fd3-d9d609ae64a7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Monopolar HF cable |
Version Model Number | 395 502 504 |
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 | 04059082026671 [Primary] |
FAS | ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04059082026671]
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 |