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Surgical Instrument

EUDAMED

Class I (EU MDR)

Ref GU.1305.14

by Gimmi GmbH

Identity

Device Name
Surgical Instrument EUDAMED
Model / Reference
GU.1305.14 EUDAMED

Identifiers

Primary DI / UDI-DI
04049047046677 EUDAMED
Basic UDI-DI
4049047LBR03ANA27DROR6 EUDAMED
Direct Marketing DI
04049047046677 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

Surgical Instrument by Gimmi 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

Manufacturer
Gimmi GmbH
EUDAMED SRN
DE-MF-000005445

Sources (1)

  • EUDAMED 47d6a0f6-a8df-4dbb-86f0-18a3232a3c6d 61 fields · synced Jul 9, 2026