FDA UDI In Commercial Distribution 🇺🇸 United States

Vitegra®

DI: 04250337119852 · Model: ICS1710FS · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vitegra®
Primary DI
04250337119852
Version / Model
ICS1710FS
Catalog Number
ICS1710FS
Company Name
Joimax GmbH
Labeler DUNS
344267187
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
1
Public Version Date
2023-01-09
Public Version Status
New
Public Device Record Key
5fb5886f-527a-459c-b6f5-cc18f763c289

Device Description

Vitegra® pro with footswitch

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
LMB Device, digital image storage, radiological

GMDN Terms

Code Name
60723 Medical image management system

Identifiers

Type ID
Primary 04250337119852

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify visual integration image capture system