Minncare HD Residual Test Strips

GUDID 30677964066888

MEDIVATORS INC.

Organic peroxy acid device sterilant, single-use
Primary Device ID30677964066888
NIH Device Record Keyc9a0a847-e2ac-4436-bb66-2c1f76830e7a
Commercial Distribution StatusIn Commercial Distribution
Brand NameMinncare HD Residual Test Strips
Version Model Number3029795
Company DUNS068199363
Company NameMEDIVATORS INC.
Device Count100
DM Exemptfalse
Pre-market Exemptfalse
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100677964066887 [Unit of Use]
GS130677964066888 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NIHDisinfectant, Subsystem, Water Purification

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2018-01-09

Devices Manufactured by MEDIVATORS INC.

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