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Everyway

FDA UDI

Class II (US FDA UDI)

by Everyway Medical Instruments Co., Ltd.

Identity

Trade Name
Everyway FDA UDI
Generic Name
Transcutaneous electrical stimulation probe FDA UDI
Device Name
Stimulator, transcutaneous electrical, aesthetic purposes FDA UDI
Model / Reference
MT-200 FDA UDI
Description
Stimulator, transcutaneous electrical, aesthetic purposes FDA UDI

Identifiers

Primary DI / UDI-DI
04719871189405 FDA UDI
510(k) Number
K142794 FDA UDI
FDA Product Code
NFO FDA UDI
GMDN Term
Transcutaneous electrical stimulation probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Transcutaneous electrical stimulation probe

Everyway by Everyway Medical Instruments Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous electrical stimulation probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Everyway Medical Instruments Co., Ltd.

Sources (1)

  • FDA UDI d92effca-a4aa-4bdf-b4e8-ea183d5c1799 34 fields · synced Jun 6, 2026