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Whitepost System DC 3 Refill

by Dentscare Ltda

Ref 4000055271

Whitepost System DC 3 Refill (4000055271) is a device classified as Class IIa in the EU and Class I in the US made by Dentscare Ltda, registered in EUDAMED on 6 May 2026 (Basic UDI-DI 78996338FGP002Y3) and listed in FDA GUDID since 1 Jun 2022 (UDI-DI 07899633827152), 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 Number78996338FGP002Y3 Basic UDI-DI 07899633827152UDI-DIDate6 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07899633827152 UDI-DI Date1 Jun 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 78996338FGP002Y3 registered 6 May 2026 Active
  • FDA GUDID UDI-DI 07899633827152 listed 1 Jun 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07899633827152
  2. Registered EUDAMED 78996338FGP002Y3

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  • Withdrawn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
Whitepost System DC 3 REFIL EUDAMED
Whitepost System GUDID
Generic name
Root canal post, preformed
Model / Ref / Catalog
4000055271, DC 3 Refill
Primary DI / UDI-DI
07899633827152
Basic UDI-DI
78996338FGP002Y3
FDA product code
ELR
EMDN code
Q010105 Reconstruction endodontic pins
GMDN term
Root canal post, preformed
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.3810
EU registration type
Standard device
EU market of registration
Portugal
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 4 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
4000055271
GUDID
DC 3 Refill
Device classEUDAMED
Class IIa
GUDID
Class I
Sterilise before useEUDAMED
No
GUDID
Yes
ImplantableEUDAMED
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 07899633827152: EUDAMED states No, FDA GUDID states Yes.

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: Root canal post, preformed

Similar devices in this category

Other devices filed under RECONSTRUCTION ENDODONTIC PINS.

Other devices from Dentscare Ltda

See all devices from Dentscare Ltda →

Properties

  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (17, all answered No)