Primary Device ID | 04059082033037 |
NIH Device Record Key | 6baf0d45-3bd7-4377-88f3-c27d7e6f2245 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trocar |
Version Model Number | 191 401 755 |
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 | true |
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 | 04059082033037 [Primary] |
HRX | Arthroscope |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04059082033037]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-04-20 |
Device Publish Date | 2018-03-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TROCAR 86526529 4812059 Live/Registered |
FERADYNE OUTDOORS, LLC 2015-02-06 |