Primary Device ID | 00840117321717 |
NIH Device Record Key | 5a44a14a-e5c8-4fe6-89ce-421ef6f71f29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Resp-O2 Air Cushion Mask with Valve, Size #4, Med Adult, (Red Hook) |
Version Model Number | 36034 |
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 | true |
Lot Batch | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840117321656 [Package] Package: Case [20 Units] In Commercial Distribution |
GS1 | 00840117321717 [Primary] |
BSJ | Mask, Gas, Anesthetic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-11 |
Device Publish Date | 2022-10-03 |
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