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Witcaremed

FDA UDI

Class II (US FDA UDI)

by Shenzhen Witcaremed Medical Technology Co., Ltd

Identity

Trade Name
WITCAREMED FDA UDI
Generic Name
Bioelectrical body composition analyser FDA UDI
Device Name
Smart Body Composition Analyzer FDA UDI
Model / Reference
BC-CA380 (white) FDA UDI
Description
Smart Body Composition Analyzer FDA UDI

Identifiers

Primary DI / UDI-DI
06976824740054 FDA UDI
FDA Product Code
PUH FDA UDI
GMDN Term
Bioelectrical body composition analyser FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2770 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bioelectrical body composition analyser

Witcaremed by Shenzhen Witcaremed Medical Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bioelectrical body composition analyser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ffaf1da-7631-4e66-bb0e-f779774ee5c9 33 fields · synced May 30, 2026