Primary Device ID | 24053613285449 |
NIH Device Record Key | b5f4c001-16ca-4896-b07a-2b176cb6aff6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trocar |
Version Model Number | 805-02-015 |
Catalog Number | 805-02-015 |
Company DUNS | 317409001 |
Company Name | Gebr. Brasseler GmbH & Co. KG |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 14053613285442 [Primary] |
GS1 | 24053613285449 [Package] Contains: 14053613285442 Package: [2 Units] In Commercial Distribution |
HTY | Pin, Fixation, Smooth |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-03 |
Device Publish Date | 2023-04-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TROCAR 86526529 4812059 Live/Registered |
FERADYNE OUTDOORS, LLC 2015-02-06 |