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Full Body Sensor Body Composition Monitor and Scale

FDA UDI

Class II (US FDA UDI)

by Omron Healthcare, Inc.

Identity

Trade Name
Full Body Sensor Body Composition Monitor and Scale FDA UDI
Generic Name
Bioelectrical body composition analyser FDA UDI
Model / Reference
HBF-516B FDA UDI

Identifiers

Primary DI / UDI-DI
00073796265168 FDA UDI
510(k) Number
K062043 FDA UDI
FDA Product Code
MNW 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bioelectrical body composition analyser

Full Body Sensor Body Composition Monitor and Scale by Omron Healthcare, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bioelectrical body composition analyser.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a5a4ec0a-4699-4ba4-a9af-a5267fddf5c1 35 fields · synced May 30, 2026