FDA UDI In Commercial Distribution 🇺🇸 United States

CURIX ORTHO REGULAR

DI: 05414904036693 · Model: CURIX ORTHO REGULAR 35X35 · AGFA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CURIX ORTHO REGULAR
Primary DI
05414904036693
Version / Model
CURIX ORTHO REGULAR 35X35
Catalog Number
3KUD1
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
4
Public Version Date
2019-06-14
Public Version Status
Update
Public Device Record Key
8e038d1e-cdfb-4929-b93e-f35a9a18baf8

Device Description

CURIX CAS US+OR REG 35X35

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IXA Cassette, radiographic film

GMDN Terms

Code Name
35437 X-ray film cassette, manual

Identifiers

Type ID
Primary 05414904036693

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K023020 000

Device Sizes

Type Value Unit Text
Width 35 Centimeter
Length 35 Centimeter