FDA UDI In Commercial Distribution 🇺🇸 United States

Genoray

DI: 08809244060601 · Model: VETERA FD · GENORAY CO., LTD.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Genoray
Primary DI
08809244060601
Version / Model
VETERA FD
Company Name
GENORAY CO., LTD.
Labeler DUNS
631064672
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-01
Public Version
1
Public Version Date
2025-12-09
Public Version Status
New
Public Device Record Key
ddd2ba9b-9bdd-451d-8020-42cbd69875ab

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
Yes
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
OWB Interventional Fluoroscopic X-Ray System

GMDN Terms

Code Name
37649 Portable general-purpose fluoroscopic x-ray system, digital

Identifiers

Type ID
Primary 08809244060601

Premarket Submissions

Submission Number Supplement Number
K230787 000