Primary Device ID | 04059082009452 |
NIH Device Record Key | d05a8d91-9a0b-4c2f-9c83-1f92fab7eb66 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trocar |
Version Model Number | 195 200 220BC |
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 | 04059082009452 [Primary] |
FDC | RESECTOSCOPE, WORKING ELEMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04059082009452]
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TROCAR 86526529 4812059 Live/Registered |
FERADYNE OUTDOORS, LLC 2015-02-06 |