← Back to catalogue

Vitalcontrol

FDA UDI

Class II (US FDA UDI)

by Beurer North America, L.p.

Identity

Trade Name
Vitalcontrol FDA UDI
Generic Name
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Device Name
Abdominal Toning Belt - EMS Electrical abdominal muscle stimulation FDA UDI
Model / Reference
SEM36 FDA UDI
Description
Abdominal Toning Belt - EMS Electrical abdominal muscle stimulation FDA UDI

Identifiers

Primary DI / UDI-DI
00853879007454 FDA UDI
FDA Product Code
NGX FDA UDI
GMDN Term
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Physical therapy transcutaneous neuromuscular electrical stimulation system

Vitalcontrol by Beurer North America, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy transcutaneous neuromuscular electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI dd9dd492-fd02-4059-9987-16d61ecfce59 34 fields · synced May 30, 2026