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Bright Posterior

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 180122502

by Dmp Dental Industry S.a.

Identity

Trade Name
Bright Posterior 0.25g x 20 A2 EUDAMED
BRIGHT POSTERIOR FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Light Curing Microhybrid Composite EUDAMED
Light curing composite. Radiopaque resin-based dental restorative material for posterior restorations. FDA UDI
Model / Reference
180122502 EUDAMED
A2, 0.25g x 20 FDA UDI
Description
Light curing composite. Radiopaque resin-based dental restorative material for posterior restorations. FDA UDI

Identifiers

Catalog Number
180122502 FDA UDI
Primary DI / UDI-DI
05206569825022 EUDAMEDFDA UDI
Basic UDI-DI
5206569COMP42SA EUDAMED
FDA Product Code
EBF FDA UDI
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Market of Registration
Greece 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

No

FDA UDI

Category: Dental composite resin

Bright Posterior by Dmp Dental Industry S.a. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI e81b7ae1-08dd-4738-bdb0-f32a8a5978c7 36 fields · synced Jun 18, 2026
  • EUDAMED ecdb80e3-a283-4db1-8bf8-ec756096ec62 61 fields · synced Jun 18, 2026