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Beurer SI30

by Beurer North America, L.P.

Beurer SI30 (603.82) is a home-use facial steamer (FDA Class I; FDA product code KFZ, Humidifier, Non-Direct Patient Interface (Home-Use)) made by Beurer North America, L.P., listed in FDA GUDID since 11 Jan 2021 (UDI-DI 00850018808217), 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 Number00850018808217 UDI-DI Date11 Jan 2021ListedStatusListed 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  • Withdrawn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
Home-use facial steamer
Model / Ref / Catalog
SI30, 603.82
Primary DI / UDI-DI
00850018808217
FDA product code
KFZ
GMDN term
Home-use facial steamer
Device class
Class I
Regulation number
868.5460
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KFZ (Humidifier, Non-Direct Patient Interface (Home-Use)).

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)