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Seal·it

EUDAMED

Class IIa (EU MDR)

Ref #821601

by Spident

Identity

Trade Name
Seal·it EUDAMED
Device Name
Seal·it EUDAMED
Model / Reference
#821601 EUDAMED

Identifiers

Primary DI / UDI-DI
08809262954418 EUDAMED
Basic UDI-DI
880926295SI3A EUDAMED
Direct Marketing DI
08809262954418 EUDAMED
EMDN Code
Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium 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

Category: Dental appliance fabrication material, ceramic

Seal·it by Spident — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Spident
EUDAMED SRN
KR-MF-000008691
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (1)

  • EUDAMED fd7f8dd6-344e-458b-9259-dcf1a614cd09 61 fields · synced Jun 18, 2026