Primary Device ID | D967300160 |
NIH Device Record Key | ae8823de-6481-438d-b883-58e6ac39eda3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Zitemp |
Version Model Number | 15g powder |
Catalog Number | 30016 |
Company DUNS | 859546940 |
Company Name | PREVEST DENPRO LIMITED |
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 | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |