FDA UDI In Commercial Distribution 🇺🇸 United States

Belifu

DI: 06970389634988 · Model: FDES115 · Famidoc Technology Co.,Ltd.
Product Codes
2
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Belifu
Primary DI
06970389634988
Version / Model
FDES115
Company Name
Famidoc Technology Co.,Ltd.
Labeler DUNS
421343701
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-17
Public Version
2
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
ef7dd0c7-86a8-4703-94c3-d4e8353d5fb4

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IPF Stimulator, Muscle, Powered
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use
35751 Transcutaneous electrical stimulation lead
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 06970389634988

Premarket Submissions

Submission Number Supplement Number
K130723 000