← Back to catalogue

Kt-1080/Ee

EUDAMED

Class I (EU MDR)

Ref 39Model KT-1080/EE

by AGA Sanitätsartikel GmbH

Identity

Trade Name
KT-1080/EE EUDAMED
Device Name
Kipptisch EUDAMED
Model / Reference
KT-1080/EE EUDAMED
39 EUDAMED

Identifiers

Primary DI / UDI-DI
04251816800483 EUDAMED
Basic UDI-DI
4251816800489H EUDAMED
Direct Marketing DI
04251816800483 EUDAMED
EMDN Code
V08060199 ELECTRIC MEDICAL BEDS - OTHER 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

Kt-1080/Ee by AGA Sanitätsartikel 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

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

Manufacturer

EUDAMED SRN
DE-MF-000005876

Sources (1)

  • EUDAMED f0cec53b-5114-4e78-9f91-0dc7eab4bea7 61 fields · synced Jul 9, 2026