DermaPrep Skin Prep Pads

GUDID 00714196392220

DERMARITE INDUSTRIES LLC

Synthetic-polymer liquid barrier dressing, non-sterile
Primary Device ID00714196392220
NIH Device Record Key632c5f79-1185-4187-b059-0fe99f009ecc
Commercial Distribution StatusIn Commercial Distribution
Brand NameDermaPrep Skin Prep Pads
Version Model Number81050
Company DUNS883925562
Company NameDERMARITE INDUSTRIES LLC
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100714196392220 [Primary]

FDA Product Code

NECBandage, Liquid, Skin Protectant

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-09-17
Device Publish Date2021-09-09

On-Brand Devices [DermaPrep Skin Prep Pads]

0071419681050281050
0071419639222081050

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