Primary Device ID | 08052141312629 |
NIH Device Record Key | 6f8357e0-538e-452e-b125-a1a506c8a5df |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterile Aspiration Tips |
Version Model Number | 22.F6061.00 |
Company DUNS | 447696675 |
Company Name | OMNIA SRL |
Device Count | 10 |
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 | false |
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 |