Primary Device ID | B504OM414810040 |
NIH Device Record Key | fe12667b-b535-47d1-9135-e6eebff07d2c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Omni Life Sc. |
Version Model Number | 4148-1004 |
Company DUNS | 016889401 |
Company Name | Provision |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 |