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Klockner 20 02 35

by Soadco, S.L.

Ref 20 02 34Model Basic UDI

Klockner 20 02 35 (20 02 34) is a device classified as Class IIa in the EU and Class I in the US made by Soadco, S.L., registered in EUDAMED on 1 Jun 2026 (Basic UDI-DI 84354516TF13QH) and listed in FDA GUDID since 18 Feb 2025 (UDI-DI 08435451661203), active as of 23 Oct 2026.

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

CE MDR

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/MDR EUDAMED Number84354516TF13QH Basic UDI-DI 08435451661203UDI-DIDate1 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08435451661203 UDI-DI Date18 Feb 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 84354516TF13QH registered 1 Jun 2026 Active
  • FDA GUDID UDI-DI 08435451661203 listed 18 Feb 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08435451661203
  2. Registered EUDAMED 84354516TF13QH

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Drill Ø2.35mm X 12mm [1 · C3] EUDAMED
Klockner GUDID
Generic name
Steel dental bur, reusable
Model / Ref / Catalog
Basic UDI, 20 02 34, 20 02 35
Primary DI / UDI-DI
08435451661203
Basic UDI-DI
84354516TF13QH
FDA product code
NDP
EMDN code
Q010399 Surgical dental devices - other
GMDN term
Steel dental bur, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
Basic UDI
20 02 34
GUDID
20 02 35
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Steel dental bur, reusable

Similar devices in this category

Other devices filed under SURGICAL DENTAL DEVICES - OTHER.

Other devices from Soadco, S.L.

See all devices from Soadco, S.L. →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)