Primary Device ID | 10815098020222 |
NIH Device Record Key | 87f0b3e4-f570-46cd-9e6a-b91e35df0a54 |
Commercial Distribution Discontinuation | 2024-08-09 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ReviveR View Configuration |
Version Model Number | DDU-C2300 |
Company DUNS | 128340200 |
Company Name | DEFIBTECH, L.L.C. |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
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 |