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Pentax Prismvue Nf2 L20s(b)

EUDAMED

Class I (EU MDR)

Ref 2037598

by HOYA Technosurgical Corporation

Identity

Trade Name
PENTAX PRISMVUE NF2 L20S(B) EUDAMED
Device Name
PENTAX Surgical Loupes EUDAMED
Model / Reference
2037598 EUDAMED

Identifiers

Primary DI / UDI-DI
04582428429824 EUDAMED
Basic UDI-DI
4582428-TSU-0001QW EUDAMED
EMDN Code
L0316 HELMETS AND BINOCULAR GLASSES FOR SURGEONS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Pentax Prismvue Nf2 L20s(b) by HOYA Technosurgical Corporation — 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

EUDAMED SRN
JP-MF-000045863
Authorised Representative
HOYA Holdings B.V. NL-AR-000004416

Sources (1)

  • EUDAMED f37f0536-d7cd-4387-a6bd-1deb59590cf2 61 fields · synced Jul 26, 2026