Sterilizing Container Trauma 010-00008

GUDID 04260029584295

MedXpert GmbH

Sterilization container Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable
Primary Device ID04260029584295
NIH Device Record Keyb438696b-7dc1-46b0-a9d2-b71f571a2355
Commercial Distribution StatusIn Commercial Distribution
Brand NameSterilizing Container Trauma
Version Model Number010-00008
Catalog Number010-00008
Company DUNS331019344
Company NameMedXpert GmbH
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de
Phone+4976345085630
Emailask-the-xpert@medXpert.de

Device Identifiers

Device Issuing AgencyDevice ID
GS104260029584295 [Primary]

FDA Product Code

MDMInstrument, Manual, Surgical, General Use

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


[04260029584295]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-05-08
Device Publish Date2017-01-05

On-Brand Devices [Sterilizing Container Trauma]

04260029585452001-20001
04260029584295010-00008

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