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Foam

EUDAMED

Class I (EU MDR)

Ref 36

by Pearl Technology AG

Identity

Device Name
Foam EUDAMED
Model / Reference
36 EUDAMED

Identifiers

Primary DI / UDI-DI
07640476390828 EUDAMED
Basic UDI-DI
764017806FoamP2 EUDAMED
Direct Marketing DI
07640476390828 EUDAMED
EMDN Code
V080302 PATIENT POSITIONING MEDICAL CUSHIONS 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

Foam by Pearl Technology Ag — 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
Pearl Technology AG
EUDAMED SRN
CH-MF-000018100
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 6723c681-56b6-44a6-95ff-1ed7362a50f3 61 fields · synced Sep 17, 2026