Primary Device ID | B504OMGS9021500320 |
NIH Device Record Key | 54cc6b4b-967b-4721-b3aa-50c51ef54244 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Brasseler |
Version Model Number | GS902.150.032 |
Company DUNS | 016889401 |
Company Name | Provision |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |
---|---|
HIBCC | B504OMGS9021500320 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-01-26 |
Device Publish Date | 2022-01-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BRASSELER 76138861 not registered Dead/Abandoned |
Gebr. Brasseler Gmbh & Co. KG 2000-09-29 |
BRASSELER 72072698 0706436 Live/Registered |
Brasseler; Peter 1959-05-01 |