MatrixPro sterilization case

GUDID 00860540000201

PRO-DEX, INC.

Sterilization/disinfection container
Primary Device ID00860540000201
NIH Device Record Keyca0b83c6-a5b0-43f3-ad50-211c61912988
Commercial Distribution StatusIn Commercial Distribution
Brand NameMatrixPro sterilization case
Version Model Number60.000.010
Company DUNS849370358
Company NamePRO-DEX, INC.
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 Numbertrue
Manufacturing Datetrue
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
GS100860540000201 [Primary]
GS110860540000208 [Package]
Package: [10 Units]
In Commercial Distribution

FDA Product Code

FRGWrap, Sterilization
KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

[00860540000201]

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Moist Heat or Steam Sterilization


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Moist Heat or Steam Sterilization


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Moist Heat or Steam Sterilization


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Moist Heat or Steam Sterilization


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Moist Heat or Steam Sterilization


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Moist Heat or Steam Sterilization


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Moist Heat or Steam Sterilization


[00860540000201]

Moist Heat or Steam Sterilization


[00860540000201]

Moist Heat or Steam Sterilization


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Moist Heat or Steam Sterilization


[00860540000201]

Moist Heat or Steam Sterilization


[00860540000201]

Moist Heat or Steam Sterilization


[00860540000201]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-06
Device Publish Date2020-03-27

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