← Back to catalogue

Feeler

EUDAMED

Class I (EU MDR)

Ref 0301-181Model 0301-180

by Meditec Source GmbH & Co. KG

Identity

Trade Name
Feeler EUDAMED
Device Name
Lenke Pfriem gerade EUDAMED
Model / Reference
0301-180 EUDAMED
0301-181 EUDAMED

Identifiers

Primary DI / UDI-DI
04262463852138 EUDAMED
Basic UDI-DI
426246385PG039K EUDAMED
EMDN Code
L091201 ORTHOPAEDIC SURGERY RASPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Feeler by Meditec Source GmbH & Co. KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000006490

Sources (1)

  • EUDAMED 4856cabb-5d3c-4e9f-ab7b-fa6c4eb72721 61 fields · synced Jul 9, 2026