Primary Device ID | 00861001002628 |
NIH Device Record Key | 88fe09e0-932b-4a71-80a7-70cad5a2afc6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Domico Med-Device, LLC |
Version Model Number | 425 |
Company DUNS | 081253414 |
Company Name | DOMICO MED-DEVICE, LLC |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |