Primary Device ID | 03700569605940 |
NIH Device Record Key | 28c24b99-4a17-4a0d-96da-f6da554df3c7 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | RDT2.8L12 |
Catalog Number | RDT2.8L12 |
Company DUNS | 263281904 |
Company Name | NEWCLIP TECHNICS |
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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |