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Detecto

FDA UDI

Class II (US FDA UDI)

by Lifespan Brands Llc

Identity

Trade Name
Detecto FDA UDI
Generic Name
Bioelectrical body composition analyser FDA UDI
Device Name
BODY COMPOSITION ANALYZER FDA UDI
Model / Reference
0185 FDA UDI
Description
BODY COMPOSITION ANALYZER FDA UDI

Identifiers

Catalog Number
D30303P0US FDA UDI
Primary DI / UDI-DI
04897077350185 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bioelectrical body composition analyser

Detecto by Lifespan Brands Llc — 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
Lifespan Brands Llc

Sources (1)

  • FDA UDI 9352e606-cdbc-47f5-b6d0-0b2202df6cb3 34 fields · synced May 30, 2026