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Antirutschmatte

EUDAMED

Class I (EU MDR)

Ref PM-7010Ref PM-7011

by Petermann GmbH

Identity

Trade Name
Antirutschmatte EUDAMED
Device Name
Non-Slip-Pad EUDAMED
Model / Reference
PM-7010 EUDAMED
PM-7011 EUDAMED

Identifiers

Primary DI / UDI-DI
04250355370105 EUDAMED
04250355370112 EUDAMED
Basic UDI-DI
42503553LARM70047011U7 EUDAMED
Direct Marketing DI
04250355370105 EUDAMED
04250355370112 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
Belgium EUDAMED
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

Antirutschmatte 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 (2)

  • EUDAMED 8d46cde1-9685-4b99-a033-7f5b38f4c064 61 fields · synced Jul 8, 2026
  • EUDAMED c82c5f76-a935-43bf-bfde-3d2aebf0e7d4 61 fields · synced May 18, 2026