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Mediana Co., Ltd. Body Composition Analyzer I20

FDA UDI

Class II (US FDA UDI)

by Mediana.CO.LTD

Identity

Trade Name
Mediana Co., Ltd. Body Composition Analyzer I20 FDA UDI
Generic Name
Bioelectrical body composition analyser FDA UDI
Model / Reference
I20M-XBXUS FDA UDI

Identifiers

Catalog Number
I20M-XBXUS FDA UDI
Primary DI / UDI-DI
08800003455928 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

No

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

Mediana Co., Ltd. Body Composition Analyzer I20 by Mediana.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

Manufacturer
Mediana.CO.LTD

Sources (1)

  • FDA UDI 085adbc3-9570-488a-b2c0-c5951c91d763 33 fields · synced Jun 6, 2026