FDA UDI In Commercial Distribution 🇺🇸 United States

CANON INC.

DI: 04960999810911 · Model: CXDI-50RF · CANON INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CANON INC.
Primary DI
04960999810911
Version / Model
CXDI-50RF
Company Name
CANON INC.
Labeler DUNS
695138065
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-09
Public Version
5
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
269b8408-3057-4601-ad9a-96c39383de0b

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JAA System, X-Ray, Fluoroscopic, Image-Intensified
IZI System, X-Ray, Angiographic
OWB Interventional Fluoroscopic X-Ray System

GMDN Terms

Code Name
17904 Computed radiography digital imaging scanner

Identifiers

Type ID
Primary 04960999810911

Customer Contacts

Phone
800-970-7227

Premarket Submissions

Submission Number Supplement Number
K092439 000