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Whitepost System DC 2 INTRO

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 4000055278

by Dentscare Ltda

Identity

Trade Name
Whitepost System DC 2 INTRO EUDAMED
Whitepost System FDA UDI
Generic Name
Root canal post, preformed FDA UDI
Device Name
Whitepost System EUDAMED
A system of intraradicular posts that are radiopaque and made of a composite reinforced with fiberglass, recommended for endodontically treated teeth. Whitepost System posts offer retention of direct and indirect materials, allowing for adequate rehabilitation. FDA UDI
Model / Reference
4000055278 EUDAMED
DC 2 Intro FDA UDI
Description
A system of intraradicular posts that are radiopaque and made of a composite reinforced with fiberglass, recommended for endodontically treated teeth. Whitepost System posts offer retention of direct and indirect materials, allowing for adequate rehabilitation. FDA UDI

Identifiers

Catalog Number
4000055278 FDA UDI
Primary DI / UDI-DI
07899633827169 EUDAMEDFDA UDI
Basic UDI-DI
78996338FGP002Y3 EUDAMED
FDA Product Code
ELR FDA UDI
DZA FDA UDI
EMDN Code
Q010105 RECONSTRUCTION ENDODONTIC PINS EUDAMED
GMDN Term
Root canal post, preformed FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.3810 FDA UDI
872.4130 FDA UDI
Market of Registration
Portugal EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Whitepost System DC 2 INTRO by Dentscare Ltda — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentscare Ltda
EUDAMED SRN
BR-MF-000004013
Authorised Representative
Nuno Flores PT-AR-000003118

Sources (2)

  • EUDAMED 449ef61a-3411-41fd-a783-e20b501d2ef3 61 fields · synced Jul 9, 2026
  • FDA UDI 49017e7c-bd77-4723-bf66-035319bd01a7 34 fields · synced May 30, 2026