Primary Device ID | 00850010197449 |
NIH Device Record Key | e8f8ecd7-3e5f-4343-9d20-7e98f57b30b9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BreathTracker |
Version Model Number | SC |
Catalog Number | QT05000-M |
Company DUNS | 874498744 |
Company Name | QUINTRON INSTRUMENT COMPANY, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
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 | false |
OTC Over-The-Counter | false |