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Prime-Dent Prime-Dent Dual Cure Composite Luting Cement

EUDAMEDFDA 510(k)

Class IIa (EU MDR)

Ref 100-100Model TF04

by Prime Dental Manufacturing

Identity

Trade Name
Prime-Dent Prime-Dent Dual Cure Composite Luting Cement EUDAMED
Device Name
Prime-Dent Dual Cure Composite Luting Cement EUDAMED
Model / Reference
TF04 EUDAMED
100-100 EUDAMED

Identifiers

Primary DI / UDI-DI
00817441022382 EUDAMED
Basic UDI-DI
081744102TF045B EUDAMED
EMDN Code
Q0101010201 DENTAL BASE CEMENTS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Prime-Dent Prime-Dent Dual Cure Composite Luting Cement by Prime Dental Manufacturing — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA 510(k)

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000008807
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (2)

  • EUDAMED 5467c258-e358-45ec-a2e5-d460ac0304b1 61 fields · synced Aug 1, 2026
  • FDA 510(k) K112574 1 fields · synced May 18, 2026