FDA UDI In Commercial Distribution 🇺🇸 United States

INTERVENTIONAL ANGIOGRAPHY SYSTEM

DI: 04987670100222 · Model: INFX-8000V · CANON MEDICAL SYSTEMS CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTERVENTIONAL ANGIOGRAPHY SYSTEM
Primary DI
04987670100222
Version / Model
INFX-8000V
Company Name
CANON MEDICAL SYSTEMS CORPORATION
Labeler DUNS
690575113
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-01
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b465917d-66e3-4848-b36a-1215f24f8678

Device Description

INTERVENTIONAL ANGIOGRAPHY SYSTEM

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
OWB Interventional fluoroscopic x-ray system
JAA System, x-ray, fluoroscopic, image-intensified
IZI System, x-ray, angiographic

GMDN Terms

Code Name
37623 Stationary angiographic x-ray system, digital

Identifiers

Type ID
Primary 04987670100222

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152696 000
K162614 000