FDA UDI In Commercial Distribution 🇺🇸 United States

Famidoc

DI: 00854314007510 · Model: FDES107 · FAMIDOC USA, INC.
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Famidoc
Primary DI
00854314007510
Version / Model
FDES107
Company Name
FAMIDOC USA, INC.
Labeler DUNS
080370811
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-29
Public Version
8
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
dd960a17-fedd-498f-9b2b-8496cab1194a

Device Description

ABDOMINAL FITNESS BELT

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
No
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

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

Identifiers

Type ID
Primary 00854314007510
Package 10854314007517

Premarket Submissions

Submission Number Supplement Number
K130723 000