Primary Device ID | 03700569610944 |
NIH Device Record Key | 3b1d8116-c3da-43a1-9110-1f81d9100f9a |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | H0.9IFT2.25L32 |
Catalog Number | H0.9IFT2.25L32 |
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 |