Primary Device ID | 10816513024887 |
NIH Device Record Key | 335b9f2e-6ca0-40e2-8365-cc92af8d116b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Set, Administration, Intravascular |
Version Model Number | EA-006-01 |
Company DUNS | 079636164 |
Company Name | MPS MEDICAL, INC |
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 | 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 |