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SISSEL® PUTTY - ivory

EUDAMED

Class I (EU MDR)

Ref 162.015Model SISSEL® PUTTY

by SISSEL GmbH

Identity

Trade Name
SISSEL® PUTTY - ivory EUDAMED
Device Name
SISSEL® PUTTY ivory flex EUDAMED
Model / Reference
SISSEL® PUTTY EUDAMED
162.015 EUDAMED

Identifiers

Primary DI / UDI-DI
04250694711355 EUDAMED
Basic UDI-DI
42506947Y0503CQ EUDAMED
Direct Marketing DI
04250694711355 EUDAMED
EMDN Code
Y0503 HANDS AND FINGERS RE-EDUCATION DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

SISSEL® PUTTY - ivory by SISSEL GmbH — 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
SISSEL GmbH
EUDAMED SRN
DE-MF-000007624

Sources (1)

  • EUDAMED 208c9352-1ffc-4cc9-bba0-799b7b67058f 61 fields · synced Jul 8, 2026