Primary Device ID | 30357515045530 |
NIH Device Record Key | 72831f22-74d3-4846-bca1-f40bd92d7041 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Benzer/UltiGuard |
Version Model Number | 09553BZ |
Company DUNS | 024723541 |
Company Name | ULTIMED, INC. |
Device Count | 100 |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |