Primary Device ID | 00810050854191 |
NIH Device Record Key | 334652ec-5826-4629-8945-0d7b4222a04f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Anesthesia Circuits |
Version Model Number | PU72 |
Company DUNS | 600850213 |
Company Name | TYPENEX MEDICAL LLC |
Device Count | 40 |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |