Primary Device ID | 04059082012919 |
NIH Device Record Key | f3b99787-06dd-4873-a124-e63b6156cf32 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bipolar HF cable |
Version Model Number | 390 805 000 |
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 | 04059082012919 [Primary] |
FAS | ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04059082012919]
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 |