Primary Device ID | 08809524497103 |
NIH Device Record Key | 7dbc25a5-d3fd-4695-8e19-1536b97dd8a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3H |
Version Model Number | 3H-820 R-S-05 |
Company DUNS | 690390383 |
Company Name | 3H, Co., Ltd |
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 | true |
Single Use | false |
Lot Batch | false |
Serial Number | true |
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 |