I'mRT MatriXX

GUDID EIBAE30300101

I'mRT MatriXX kalibriert

IBA Dosimetry GmbH

Accelerator system quality assurance device
Primary Device IDEIBAE30300101
NIH Device Record Key5f7da44a-27c4-4995-a65d-5efcedd1e933
Commercial Distribution StatusIn Commercial Distribution
Brand NameI'mRT MatriXX
Version Model NumberE3030010
Company DUNS332599307
Company NameIBA Dosimetry GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com
Phone+49912860738
Emailservice@iba-group.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEIBAE30300100 [Primary]
HIBCCEIBAE30300101 [Package]
Contains: EIBAE30300100
Package: Aluminium case [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYEAccelerator, Linear, Medical

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 Date2016-09-09