Primary Device ID | 30809160023147 |
NIH Device Record Key | 8df99d08-f81d-4f36-9642-b3d1a63fec39 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SafeTCount™ |
Version Model Number | 3200 |
Company DUNS | 092364462 |
Company Name | MEDICAL ACTION INDUSTRIES INC. |
Device Count | 100 |
DM Exempt | true |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10809160023143 [Unit of Use] |
GS1 | 20809160023140 [Primary] |
GS1 | 30809160023147 [Package] Contains: 20809160023140 Package: [5 Units] In Commercial Distribution |
LWH | Counter, sponge, surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2016-08-20 |
20809160448660 - Medical Action Industries | 2024-12-17 |
20809160448011 - Medical Action Industries | 2024-12-13 |
20809160448028 - Medical Action Industries | 2024-12-13 |
20809160447052 - Medical Action Industries | 2024-12-05 |
20809160447069 - Medical Action Industries | 2024-12-05 |
20809160444532 - Clear Sequence | 2024-11-26 |
20809160444266 - Medical Action Industries | 2024-11-25 |
20809160442682 - Medical Action Industries | 2024-11-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SAFETCOUNT 76586063 not registered Dead/Abandoned |
Medical Action Industries Inc. 2004-04-08 |
SAFETCOUNT 74067335 1645092 Dead/Cancelled |
Sage Products, Inc. 1990-06-11 |