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Beurer BR60

by Beurer North America, L.P.

Beurer BR60 (607.58) is a Class II device made by Beurer North America, L.P., listed in FDA GUDID since 7 Dec 2020 (UDI-DI 00850018808224), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850018808224 UDI-DI Date7 Dec 2020ListedStatusListed 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  • Withdrawn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
Insect bite/sting hyperthermia device
Model / Ref / Catalog
BR60, 607.58
Primary DI / UDI-DI
00850018808224
FDA product code
IRT
GMDN term
Insect bite/sting hyperthermia device
Device class
Class II
Regulation number
890.5740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Insect bite/sting hyperthermia device

Similar devices

Other devices filed under FDA product code IRT (Pad, Heating, Powered).

Other devices from Beurer North America, L.P.

See all devices from Beurer North America, L.P. →

Properties

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