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Farrior ear speculum M1018601

by Spiggle & Theis Medizintechnik GmbH

Farrior ear speculum M1018601 is a Class I device made by Spiggle & Theis Medizintechnik GmbH, listed in FDA GUDID since 28 Oct 2026 (UDI-DI 04250676750662), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250676750662 UDI-DI Date28 Oct 2026ListedStatusListed 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  • Withdrawn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
Farrior ear speculum
Generic name
Ear speculum, reusable
Model / Ref / Catalog
M1018601
Description
size 1, straight, round OD 4.3 mm, ID 3.3 mm
Primary DI / UDI-DI
04250676750662
FDA product code
EPY
GMDN term
Ear speculum, reusable
Device class
Class I
Regulation number
878.1800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Spiggle & Theis Medizintechnik GmbH

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)