FDA UDI In Commercial Distribution 🇺🇸 United States

SCENARIA View

DI: 04573596200544 · Model: SCENARIA View · FUJIFILM CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
SCENARIA View
Primary DI
04573596200544
Version / Model
SCENARIA View
Catalog Number
SCENARIA View
Company Name
FUJIFILM CORPORATION
Labeler DUNS
680160734
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-14
Public Version
4
Public Version Date
2025-05-23
Public Version Status
Update
Public Device Record Key
6c3be672-3335-4dfb-890e-b5b8ad399ee1

Device Description

Full-body CT system

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
JAK System, X-Ray, Tomography, Computed

GMDN Terms

Code Name
37618 Full-body CT system

Identifiers

Type ID
Primary 04573596200544
Previous 04580292766694