Primary Device ID | 00841470110055 |
NIH Device Record Key | d4ddbba4-0fbf-4b9d-95b4-9641e8a23647 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aero-Pro HEPA Light Machine |
Version Model Number | 201022 |
Company DUNS | 030619483 |
Company Name | PULMODYNE INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841470110055 [Primary] |
GS1 | 10841470110052 [Package] Package: [50 Units] In Commercial Distribution |
CAH | Filter, Bacterial, Breathing-Circuit |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-04 |
Device Publish Date | 2020-04-24 |
10841470105454 - HMEF | 2024-07-09 |
10841470105461 - HMEF | 2024-07-09 |
10841470105478 - HMEF | 2024-07-09 |
10841470105485 - HMEF | 2024-07-09 |
10841470100718 - VT Select | 2023-04-18 |
10841470100749 - VT Select | 2023-04-18 |
10841470100770 - VT Select | 2023-04-18 |
10841470100794 - VT Select | 2023-04-18 |