FDA UDI In Commercial Distribution 🇺🇸 United States

acculove

DI: 00818218024813 · Model: FDES108 · Famidoc Technology Co.,Ltd.
Product Codes
2
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
acculove
Primary DI
00818218024813
Version / Model
FDES108
Company Name
Famidoc Technology Co.,Ltd.
Labeler DUNS
421343701
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-25
Public Version
7
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
342a63fa-f14d-4892-861d-3c2d692468b5

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

GMDN Terms

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

Identifiers

Type ID
Primary 00818218024813

Premarket Submissions

Submission Number Supplement Number
K113010 000