Primary Device ID | 08800046040822 |
NIH Device Record Key | a54173de-e3c6-4a89-ab04-d068b5ccf1e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ASS423-7U |
Version Model Number | ASS423-7U |
Company DUNS | 694828541 |
Company Name | GNI Co.,Ltd |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |