FDA UDI In Commercial Distribution 🇺🇸 United States

Allia

DI: 00198953052488 · Model: Moveo · GE MEDICAL SYSTEMS
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Allia
Primary DI
00198953052488
Version / Model
Moveo
Catalog Number
5981876
Company Name
GE MEDICAL SYSTEMS
Labeler DUNS
266062561
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-17
Public Version
1
Public Version Date
2025-12-25
Public Version Status
New
Public Device Record Key
6c4396db-353e-459b-a5ff-5b982a44d58c

Device Description

Allia Moveo UDI

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
37623 Stationary angiographic x-ray system, digital

Identifiers

Type ID
Primary 00198953052488

Premarket Submissions

Submission Number Supplement Number
K251199 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
20 – 80 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 103 KiloPascal