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Beurer BR70

by Beurer North America, L.P.

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810110200562 UDI-DI Date9 Jun 2026ListedStatusListed GUDID: not in commercial distribution

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  • Withdrawn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
BR70, 611.14
Primary DI / UDI-DI
00810110200562
FDA Product Code
IRT
GMDN Term
Insect bite/sting hyperthermia device
Device Class
Class II
Regulation Number
890.5740
GUDID distribution status
Not in Commercial Distribution

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 (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No