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LLD lead cutter

EUDAMED

Class IIa (EU MDR)

Ref 518-024

by Philips Image Guided Therapy Corporation

Identity

Trade Name
LLD lead cutter EUDAMED
Device Name
LLD lead cutter EUDAMED
Model / Reference
518-024 EUDAMED

Identifiers

Primary DI / UDI-DI
00813132029654 EUDAMED
Basic UDI-DI
081313202BM887NC EUDAMED
EMDN Code
C01901903 VESSEL HARVESTING SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

LLD lead cutter by Philips Image Guided Therapy Corporation — Class IIa — 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

EUDAMED SRN
US-MF-000018632
Authorised Representative
Philips Medical Systems Nederland B.V. NL-AR-000001422

Sources (1)

  • EUDAMED 496fb0f6-0670-409c-a6d7-5bd521027585 61 fields · synced Jul 19, 2026