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Echolight S.p.a.

FDA UDI

Class II (US FDA UDI)

by Echolight Spa

Identity

Trade Name
Echolight S.p.a. FDA UDI
Generic Name
Bioelectrical body composition analyser FDA UDI
Model / Reference
EchoS FDA UDI

Identifiers

Primary DI / UDI-DI
08052461860022 FDA UDI
510(k) Number
K202514 FDA UDI
FDA Product Code
MUA FDA UDI
OMV FDA UDI
GMDN Term
Bioelectrical body composition analyser FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1180 FDA UDI
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

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

Category: Bioelectrical body composition analyserBone absorptiometric ultrasound system

Echolight S.p.a. by Echolight Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone absorptiometric ultrasound system.

Cleared under the same submission

K202514 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Echolight Spa

Sources (1)

  • FDA UDI a05f5c61-36ca-404a-943f-2a62a79742a0 33 fields · synced May 30, 2026