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Scissors 10-533-10 TAN

by Spiggle & Theis Medizintechnik GmbH

Scissors 10-533-10 TAN is a Class I device made by Spiggle & Theis Medizintechnik GmbH, listed in FDA GUDID since 12 Sep 2022 (UDI-DI 04250381869963), 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 Number04250381869963 UDI-DI Date12 Sep 2022ListedStatusListed 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  • Withdrawn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
Scissors
Generic name
Ear scissors, reusable
Model / Ref / Catalog
10-533-10 TAN
Description
curved, pointed, fine 10.5 cm, black coated
Primary DI / UDI-DI
04250381869963
FDA product code
LRC
GMDN term
Ear scissors, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ear scissors, reusable

Similar devices in this category

Other devices filed under Ear scissors, reusable.

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)