Primary Device ID | 00840117300019 |
NIH Device Record Key | 205caecc-a340-4486-b79c-c8f773a53cb3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | My Doggy Compressor Nebulizer |
Version Model Number | 5608DG |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
Device Count | 4 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00616784560854 [Unit of Use] |
GS1 | 00840117300019 [Primary] |
CAF | Nebulizer (Direct Patient Interface) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-26 |
Device Publish Date | 2019-12-18 |
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00840117340527 - Resp-O2 Disposable Guedel Airway,60 mm, Toddler, Black | 2024-12-09 |
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