CVS Liquid Bandage Spray

GUDID 10050428617653

Liquid Bandage in aerosol can

WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Skin-cover sealant
Primary Device ID10050428617653
NIH Device Record Key2e53328f-7255-484a-a1c5-2b7292b63cd1
Commercial Distribution StatusIn Commercial Distribution
Brand NameCVS Liquid Bandage Spray
Version Model Number276670
Company DUNS062312574
Company NameWOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100050428617656 [Primary]
GS110050428617653 [Package]
Contains: 00050428617656
Package: Case [48 Units]
In Commercial Distribution

FDA Product Code

NECBandage, Liquid, Skin Protectant

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-23
Device Publish Date2020-01-15

Devices Manufactured by WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

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