Primary Device ID | 10709078003612 |
NIH Device Record Key | 2d7436aa-9a16-4ff6-845f-7cb7296fdb2a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Composite Respiratory Kit |
Version Model Number | 0767 |
Company DUNS | 092673953 |
Company Name | WESTMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |