Sterilizing Container Trauma 001-20001

GUDID 04260029585452

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 ID	04260029585452
NIH Device Record Key	d936a13b-daf6-4c3a-ab24-be54af2f0d72
Commercial Distribution Status	In Commercial Distribution
Brand Name	Sterilizing Container Trauma
Version Model Number	001-20001
Catalog Number	001-20001
Company DUNS	331019344
Company Name	MedXpert GmbH
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de
Phone	+4976345085630
Email	ask-the-xpert@medXpert.de

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260029585452 [Primary]

FDA Product Code

MDM	Instrument, Manual, Surgical, General Use