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Diamond Fibrelight Handle / Standard

EUDAMED

Class I (EU MDR)

Ref 50525

by Penlon Limited

Identity

Trade Name
Diamond Fibrelight Handle / Standard EUDAMED
Device Name
Laryngoscope handle, reusable EUDAMED
Model / Reference
50525 EUDAMED

Identifiers

Primary DI / UDI-DI
05051977001892 EUDAMED
Basic UDI-DI
5051977LAR-RUHLYF EUDAMED
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Category: Laryngoscope blade, reusable

Diamond Fibrelight Handle / Standard by Penlon Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Penlon Limited
EUDAMED SRN
GB-MF-000025115
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 1db273dd-e5b6-49ba-92b3-60536f67cd09 61 fields · synced Jul 25, 2026