Skip to content

Well-Root PT WT202-K000

by Vericom Co., Ltd.

Ref WT202-K000

Well-Root PT WT202-K000 is a device classified as Class IIa in the EU and Class II in the US made by Vericom Co., Ltd., registered in EUDAMED on 23 Oct 2026 (Basic UDI-DI B-08809254459419) and listed in FDA GUDID since 27 Nov 2025 (UDI-DI 08809254459419), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-08809254459419 Basic UDI-DI 08809254459419UDI-DIDate23 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08809254459419 UDI-DI Date27 Nov 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-08809254459419 registered 23 Oct 2026 Active
  • FDA GUDID UDI-DI 08809254459419 listed 27 Nov 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08809254459419
  2. Registered EUDAMED B-08809254459419

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  • Withdrawn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
Well-Root PT
Generic name
Hygroscopic dental cement
Model / reference
WT202-K000
Primary DI / UDI-DI
08809254459419
Basic UDI-DI
B-08809254459419
FDA product code
KIF
EMDN code
Q01010201 Root canal filling dental pastes
GMDN term
Hygroscopic dental cement
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3820
EU registration type
Legacy device (under a directive)
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

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

Similar devices in this category

Other devices filed under ROOT CANAL FILLING DENTAL PASTES.

Other devices from Vericom Co., Ltd.

See all devices from Vericom Co., Ltd. →

Properties

  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (17, all answered No)