Primary Device ID | 00372217000013 |
NIH Device Record Key | bc951a38-f6b3-440f-ba4e-d6e0c44b1594 |
Commercial Distribution Discontinuation | 2018-12-15 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Pro-Care Nebulizer Easy |
Version Model Number | Easy |
Company DUNS | 081149273 |
Company Name | ARISE MEDICAL LLC |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00372217000013 [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 | 2019-01-01 |
Device Publish Date | 2018-12-01 |
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