Primary Device ID | 30681066053707 |
NIH Device Record Key | f44e1ef6-4056-4115-83d9-74d018a6b106 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | THE SOLUTION |
Version Model Number | 160THCDCA06 |
Company DUNS | 086413028 |
Company Name | Sakar International, Inc. |
Device Count | 2 |
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 | false |
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 | 00681066053706 [Primary] |
GS1 | 30681066053707 [Unit of Use] |
NFT | Test, Amphetamine, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-20 |
Device Publish Date | 2022-07-12 |
30681066053998 | 139AUCMUC03 |
30681066053707 | 160THCDCA06 |
30681066049601 | 105THCSTR03 |
30021331054501 | 150AUCMUC14 |