FDA UDI In Commercial Distribution 🇺🇸 United States

Aurora

DI: 00195278878502 · Model: SPECT with Revolution Ascend CT · G E MEDICAL SYSTEMS ISRAEL LTD.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aurora
Primary DI
00195278878502
Version / Model
SPECT with Revolution Ascend CT
Company Name
G E MEDICAL SYSTEMS ISRAEL LTD.
Labeler DUNS
532102365
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-25
Public Version
3
Public Version Date
2026-01-30
Public Version Status
Update
Public Device Record Key
a4aee6ec-a9ed-43ff-971c-79caace10d4b

Device Description

AURORA NM GANTRY FINAL

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
KPS System, Tomography, Computed, Emission

GMDN Terms

Code Name
37618 Full-body CT system
40640 Stationary gamma camera system

Identifiers

Type ID
Primary 00195278878502