← Back to catalogue

92301700002

EUDAMED

Class I (EU MDR)

Ref 92301700002Model 43017

by Glaswarenfabrik Karl Hecht GmbH & Co KG

Identity

Model / Reference
43017 EUDAMED
92301700002 EUDAMED

Identifiers

Primary DI / UDI-DI
04251054449772 EUDAMED
Basic UDI-DI
4251054443017RG 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

No

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

92301700002 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000006553

Sources (1)

  • EUDAMED aa40ff2e-7d61-4ceb-aa4b-0014f98077d3 61 fields · synced Oct 6, 2026