Primary Device ID | 00813830023916 |
NIH Device Record Key | ba83e86d-5807-47d2-b185-87e70dc17791 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flowmeter, Digital Pkg G, Biewer |
Version Model Number | 56600-BWR |
Catalog Number | 56600-BWR |
Company DUNS | 088302096 |
Company Name | ACCUTRON, 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 | false |
Lot Batch | true |
Serial Number | true |
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 |