FDA UDI In Commercial Distribution 🇺🇸 United States

MatriXX Evolution kalibriert

DI: EIBAE30300120 · Model: E3030012 · IBA Dosimetry GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MatriXX Evolution kalibriert
Primary DI
EIBAE30300120
Version / Model
E3030012
Company Name
IBA Dosimetry GmbH
Labeler DUNS
332599307
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
3
Public Version Date
2020-08-10
Public Version Status
Update
Public Device Record Key
ced7d872-3aa7-4a55-acd3-30f0870cde68

Device Description

MatriXX Evolution kalibriert

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYE Accelerator, Linear, Medical

GMDN Terms

Code Name
38399 Accelerator system quality assurance device

Identifiers

Type ID
Package EIBAE30300121
Primary EIBAE30300120

Customer Contacts

Phone
+49912860738

Premarket Submissions

Submission Number Supplement Number
K072374 000