FDA UDI In Commercial Distribution 🇺🇸 United States

Revolution

DI: 00840682138796 · Model: 160mm Detector Upgrade · GE MEDICAL SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Revolution
Primary DI
00840682138796
Version / Model
160mm Detector Upgrade
Company Name
GE MEDICAL SYSTEMS, INC.
Labeler DUNS
809785715
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-11
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
dbb7ec40-acd8-4da6-901d-a690062ac0d1

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 00840682138796

Premarket Submissions

Submission Number Supplement Number
K163213 000