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Beurer

FDA UDI

Class II (US FDA UDI)

by Beurer North America, L.p.

Identity

Trade Name
Beurer FDA UDI
Generic Name
Bioelectrical body composition analyser FDA UDI
Device Name
Body Fat Scale FDA UDI
Model / Reference
BF221 (Art.-No. 740.79) FDA UDI
Description
Body Fat Scale FDA UDI

Identifiers

Catalog Number
Type BF220 FDA UDI
Primary DI / UDI-DI
00852547004269 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

Yes

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

Beurer by Beurer North America, L.p. — 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

Sources (1)

  • FDA UDI 8c02f8f8-058f-4e5f-a5e7-a6ebf15bfabc 36 fields · synced May 30, 2026