FDA UDI In Commercial Distribution 🇺🇸 United States

DX-M

DI: 05414904050385 · Model: 5170/200 · AGFA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DX-M
Primary DI
05414904050385
Version / Model
5170/200
Catalog Number
E4YW2
Company Name
AGFA
Labeler DUNS
374444883
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-01
Public Version
7
Public Version Date
2019-06-14
Public Version Status
Update
Public Device Record Key
8386097c-8ba2-4826-b2e6-08b1ee04e324

Device Description

DX-M DIGITIZER

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
MUE Full field digital,system,x-ray,mammographic

GMDN Terms

Code Name
17904 Computed radiography digital imaging scanner

Identifiers

Type ID
Primary 05414904050385

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111324 000