Primary Device ID | 00817081022629 |
NIH Device Record Key | c04dd9ec-0e82-4c2e-bb61-3562ae135c7b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PFT Kit E, VBMax36E |
Version Model Number | PFT Kit E, VBMax36E - 189166 |
Catalog Number | 189166 |
Company DUNS | 020275145 |
Company Name | A-M SYSTEMS, LLC |
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 | true |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |