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Spekulum, vaginal / Speculum, vaginal

EUDAMED

Class I (EU MDR)

Ref 71291-00

by REDA Instrumente GmbH

Identity

Device Name
Spekulum, vaginal / Speculum, vaginal EUDAMED
Model / Reference
71291-00 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058055374 EUDAMED
Basic UDI-DI
40630580000017445 EUDAMED
Direct Marketing DI
04063058055374 EUDAMED
EMDN Code
L059001 VAGINAL SPECULUMS, 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

Category: Vaginal speculum, reusable

Spekulum, vaginal / Speculum, vaginal by REDA Instrumente GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal speculum, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000005592

Sources (1)

  • EUDAMED e571626e-a696-4c2a-a83d-1da11266fed1 61 fields · synced Sep 18, 2026