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BodiMetrics

FDA UDI

Class II (US FDA UDI)

by Shenzhen Viatom Technology Co., Ltd.

Identity

Trade Name
BodiMetrics FDA UDI
Generic Name
Multiple physiological parameter spot-check system, home-use FDA UDI
Model / Reference
VitalsRX Health Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
06934440100713 FDA UDI
510(k) Number
K150869 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
Multiple physiological parameter spot-check system, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 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

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Multiple physiological parameter spot-check system, home-use

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

Similar devices

Also classified as Multiple physiological parameter spot-check system, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shenzhen Viatom Technology Co., Ltd.

Sources (1)

  • FDA UDI e327f993-e9f5-4d88-bba2-d3e1db7c3037 33 fields · synced Jun 8, 2026