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P Pro Crown & Bridge A1

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 019.3062Model Dental Composites and Accessories - Temporary Materials

by Deltamed GmbH

Identity

Trade Name
P Pro Crown & Bridge A1 EUDAMEDFDA UDI
Generic Name
Temporary dental crown/bridge resin FDA UDI
Device Name
P pro Crown & Bridge A1 1000g FDA UDI
Model / Reference
Dental Composites and Accessories - Temporary Materials EUDAMED
019.3062 EUDAMEDFDA UDI
Description
P pro Crown & Bridge A1 1000g FDA UDI

Identifiers

Catalog Number
019.3062 FDA UDI
Primary DI / UDI-DI
04260635980269 EUDAMEDFDA UDI
Basic UDI-DI
++EDELTD03BUDI030022GF EUDAMED
Direct Marketing DI
04260635980269 EUDAMED
510(k) Number
K200039 FDA UDI
FDA Product Code
EBG FDA UDI
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED
GMDN Term
Temporary dental crown/bridge resin FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3770 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental composite resin

P Pro Crown & Bridge A1 by DeltaMed GmbH — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Deltamed GmbH
EUDAMED SRN
DE-MF-000007882

Sources (2)

  • EUDAMED a8ba9411-455c-44b7-98e3-0db87098ca48 61 fields · synced Jul 9, 2026
  • FDA UDI 262cc245-bf44-4c37-8178-829e5c94a005 36 fields · synced May 30, 2026