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I-SiL BITE

EUDAMED

Class I (EU MDR)

Ref #7511P02

by Spident

Identity

Trade Name
I-SiL BITE EUDAMED
Device Name
I-SiL BITE EUDAMED
Model / Reference
#7511P02 EUDAMED

Identifiers

Primary DI / UDI-DI
08809262955088 EUDAMED
Basic UDI-DI
880926295IBZT EUDAMED
Direct Marketing DI
08809262955088 EUDAMED
EMDN Code
Q01020102 DENTAL IMPRESSION VINYLSILOXANS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Bulgaria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

I-SiL BITE by Spident — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

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 07aa3f4b-797c-4da7-8ae1-c2e5c9c05f84 61 fields · synced May 22, 2026