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Spekulum, vaginal / Speculum, vaginal

EUDAMED

Class I (EU MDR)

Ref 71313-30

by REDA Instrumente GmbH

Identity

Device Name
Spekulum, vaginal / Speculum, vaginal EUDAMED
Model / Reference
71313-30 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058055770 EUDAMED
Basic UDI-DI
40630580000017445 EUDAMED
Direct Marketing DI
04063058055770 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

Spekulum, vaginal / Speculum, vaginal by REDA Instrumente GmbH — 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
DE-MF-000005592

Sources (1)

  • EUDAMED f2c785ea-db94-468c-9c95-eb1c44b06c6f 61 fields · synced Aug 2, 2026