Primary Device ID | 00840117310124 |
NIH Device Record Key | 8f26de1f-ce96-477b-a1ca-eba4f005987b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Resp-O2 Oxygen Regulator, CGA 870 Style |
Version Model Number | 36360 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
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 | false |
Device Combination Product | false |
Single Use | false |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |