Primary Device ID | 10818674021446 |
NIH Device Record Key | 2a82342c-6c7c-44b1-a49c-48f04dd2f2ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FlipCutter® III Drill |
Version Model Number | AR-1204FF |
Catalog Number | 144000ar |
Company DUNS | 534123013 |
Company Name | T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION |
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 | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | true |
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 | 10818674021446 [Primary] |
HTO | Reamer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-25 |
Device Publish Date | 2024-01-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLIPCUTTER 77673614 3672945 Live/Registered |
Arthrex, Inc. 2009-02-19 |