Electrode Skin Prep Pads

GUDID 00616784150819

DYNAREX CORPORATION

Electrode skin abrasion pad
Primary Device ID00616784150819
NIH Device Record Keycc2a4b7f-f19d-4108-a58d-90517e8e4574
Commercial Distribution StatusIn Commercial Distribution
Brand NameElectrode Skin Prep Pads
Version Model Number1508
Company DUNS008124539
Company NameDYNAREX CORPORATION
Device Count100
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 Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100616784150819 [Unit of Use]
GS100616784150826 [Primary]

FDA Product Code

KOYDegreaser, Skin, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-18
Device Publish Date2022-05-10

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