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ChoiceMMed

FDA UDI

Class II (US FDA UDI)

by Beijing Choice Electronic Technology Co., Ltd.

Identity

Trade Name
ChoiceMMed FDA UDI
Generic Name
Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Device Name
Electronic Pulse Stimulator FDA UDI
Model / Reference
CTSW2A1 FDA UDI
Description
Electronic Pulse Stimulator FDA UDI

Identifiers

Primary DI / UDI-DI
00846841013973 FDA UDI
FDA Product Code
NYN FDA UDI
NGX FDA UDI
NUH FDA UDI
GMDN Term
Analgesic transcutaneous electrical nerve stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Analgesic transcutaneous electrical nerve stimulation system

ChoiceMMed by Beijing Choice Electronic Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analgesic transcutaneous electrical nerve stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beijing Choice Electronic Technology Co., Ltd.

Sources (1)

  • FDA UDI ea6f43f8-c385-487a-925e-4e25d99f7524 33 fields · synced May 30, 2026