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Beurer BF221 (Art.-No. 740.79)

by Beurer North America, L.P.

Beurer BF221 (Art.-No. 740.79) (Type BF220) is a Class II device made by Beurer North America, L.P., listed in FDA GUDID since 15 Mar 2017 (UDI-DI 00852547004269), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00852547004269 UDI-DI Date15 Mar 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Beurer
Generic name
Bioelectrical body composition analyser
Model / Ref / Catalog
BF221 (Art.-No. 740.79), Type BF220
Primary DI / UDI-DI
00852547004269
FDA product code
PUH
GMDN term
Bioelectrical body composition analyser
Device class
Class II
Regulation number
870.2770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bioelectrical body composition analyser

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Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)