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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
Electrocardiographic monitor FDA UDI
Device Name
Handheld ECG Monitor FDA UDI
Model / Reference
MD100B2 FDA UDI
Description
Handheld ECG Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
06942820461095 FDA UDI
FDA Product Code
DPS FDA UDI
GMDN Term
Electrocardiographic monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2340 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

Yes

FDA UDI

Over-the-Counter

No

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
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic monitor

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 Electrocardiographic monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 318b2d33-979d-4980-b398-7450958b13dd 33 fields · synced Jun 1, 2026