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Kruidvat Sensation

EUDAMED

Class IIb (EU MDR)

Ref PM01

by Ttk Healthcare Limited - Protective Devices Division

Identity

Trade Name
KRUIDVAT SENSATION EUDAMED
Device Name
Condom EUDAMED
Model / Reference
PM01 EUDAMED

Identifiers

Primary DI / UDI-DI
08906007137249 EUDAMED
Basic UDI-DI
B-08906007137249 EUDAMED
EMDN Code
U110101 CONDOMS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Kruidvat Sensation by Ttk Healthcare Limited - Protective Devices Division — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IN-MF-000008508
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (1)

  • EUDAMED 3e4a4e1b-76b9-460b-a3ac-d63e87347c9f 61 fields · synced Jun 19, 2026