FDA UDI In Commercial Distribution 🇺🇸 United States

Revolution

DI: 00840682146197 · Model: ACT LMB · GE Hualun Medical Systems Co., Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Revolution
Primary DI
00840682146197
Version / Model
ACT LMB
Company Name
GE Hualun Medical Systems Co., Ltd
Labeler DUNS
554408665
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-25
Public Version
2
Public Version Date
2026-03-02
Public Version Status
Update
Public Device Record Key
b5736d77-c980-4e14-b45c-e37c725a676d

Device Description

Revolution ACT designated medical device for Cannon Tube

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 00840682146197

Premarket Submissions

Submission Number Supplement Number
K171013 000