FDA UDI In Commercial Distribution 🇺🇸 United States

accufit

DI: 00816864021682 · Model: accufit · METTLER ELECTRONICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
accufit
Primary DI
00816864021682
Version / Model
accufit
Company Name
METTLER ELECTRONICS CORP.
Labeler DUNS
008513913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-22
Public Version
1
Public Version Date
2026-04-30
Public Version Status
New
Public Device Record Key
8236f3ce-a669-4600-9816-20bb3600ce3b

Device Description

Indications for Use: - Relaxation of muscle spasms - Prevention or retardation of disuse atrophy - Increase local blood circulation - Muscle re-education - Maintaining or increasing range of motion - Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis - Improvement of abdominal tone, for strengthening of the abdominal muscles, for development of firmer abdomen. - Improvement of muscle tone and firmness, for strengthening muscles in arms, thighs and buttocks areas.

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
IPF Stimulator, Muscle, Powered

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00816864021682

Premarket Submissions

Submission Number Supplement Number
K233926 000