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Scissors 10-531-10

by Spiggle & Theis Medizintechnik GmbH

Ref 10-531-10

Scissors 10-531-10 is a Class I device made by Spiggle & Theis Medizintechnik GmbH, registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI B-04250676745149) and listed in FDA GUDID since 3 Sep 2025 (UDI-DI 04250676745149), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04250676745149 Basic UDI-DI 04250676745149UDI-DIDate30 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250676745149 UDI-DI Date3 Sep 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250676745149 registered 30 Sep 2026 Active
  • FDA GUDID UDI-DI 04250676745149 listed 3 Sep 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250676745149
  2. Registered EUDAMED B-04250676745149

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Scissors
Generic name
Ear scissors, reusable
Model / Ref / Catalog
10-531-10
Description
straight, pointed, very fine 10.5 cm
Primary DI / UDI-DI
04250676745149
Basic UDI-DI
B-04250676745149
FDA product code
JZB
EMDN code
L010499 Surgical scissors, reusable - other
GMDN term
Ear scissors, reusable
Device class
Class I
Regulation number
874.4420
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Sterilise before useEUDAMED
Yes
GUDID
No

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 04250676745149: EUDAMED states Yes, FDA GUDID states No.

Related devices

Category: Ear scissors, reusable

Similar devices in this category

Other devices filed under SURGICAL SCISSORS, REUSABLE - OTHER.

Other devices from Spiggle & Theis Medizintechnik GmbH

See all devices from Spiggle & Theis Medizintechnik GmbH →

Properties

  • Sterilise before use YesEUDAMEDNoGUDID
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)