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I-SiL Putty

EUDAMED

Class I (EU MDR)

Ref #7409P02

by Spident

Identity

Trade Name
I-SiL Putty EUDAMED
Device Name
I-Sil Putty EUDAMED
Model / Reference
#7409P02 EUDAMED

Identifiers

Primary DI / UDI-DI
08809262955040 EUDAMED
Basic UDI-DI
880926295PU3R EUDAMED
Direct Marketing DI
08809262955040 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

Category: Silicone dental impression material

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

Similar devices

Also classified as Silicone dental impression material.

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 766283b9-1286-4830-a9e3-8de36e86007d 61 fields · synced May 29, 2026