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42887020

EUDAMED

Class I (EU MDR)

Ref 42887020Model 42885

by Glaswarenfabrik Karl Hecht GmbH & Co KG

Identity

Model / Reference
42885 EUDAMED
42887020 EUDAMED

Identifiers

Primary DI / UDI-DI
04251054428333 EUDAMED
Basic UDI-DI
4251054442885T2 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

42887020 by Glaswarenfabrik Karl Hecht GmbH & Co KG — 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-000006553

Sources (1)

  • EUDAMED e5807f09-4fdd-4da5-869a-e3e965c35e70 61 fields · synced Jun 19, 2026