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Pentax Prismvue Nf2 T30s(s)

EUDAMED

Class I (EU MDR)

Ref 2037930

by HOYA Technosurgical Corporation

Identity

Trade Name
PENTAX PRISMVUE NF2 T30S(S) EUDAMED
Device Name
PENTAX Surgical Loupes EUDAMED
Model / Reference
2037930 EUDAMED

Identifiers

Primary DI / UDI-DI
04582428448252 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

Category: Surgical binoculars, reusable

Pentax Prismvue Nf2 T30s(s) by HOYA Technosurgical Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical binoculars, reusable.

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 b4eead35-b1ad-4f79-8e61-9c770ada0afe 61 fields · synced Jul 31, 2026