Primary Device ID | 00050428309452 |
NIH Device Record Key | 45195e9c-249c-47f2-abb4-2bde29ecf2a1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CVS |
Version Model Number | GUL540 |
Company DUNS | 062312574 |
Company Name | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
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 |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com | |
Phone | 508-490-7250 |
Stagg@helenoftroy.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00050428309452 [Primary] |
GS1 | 70328785995403 [Package] Package: case [2 Units] In Commercial Distribution |
KFZ | Humidifier, Non-Direct Patient Interface (Home-Use) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-12-11 |
Device Publish Date | 2020-12-03 |
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