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Caremaster XL

EUDAMED

Class I (EU MDR)

Ref PM-2097

by Petermann GmbH

Identity

Trade Name
Caremaster XL EUDAMED
Device Name
Caremaster EUDAMED
Model / Reference
PM-2097 EUDAMED

Identifiers

Primary DI / UDI-DI
04250355320971 EUDAMED
Basic UDI-DI
42503553OOGM209520974E EUDAMED
Direct Marketing DI
04250355320971 EUDAMED
EMDN Code
Y99 DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - OTHER 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

Caremaster XL by Petermann 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
Petermann GmbH
EUDAMED SRN
DE-MF-000013598

Sources (1)

  • EUDAMED 7f387315-367b-46c7-92b7-b542ba80e252 61 fields · synced Jun 19, 2026