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Lecco X-Large

EUDAMED

Class I (EU MDR)

Ref 870.04Model STRETCHERS

by KONG S.p.A.

Identity

Trade Name
LECCO X-LARGE EUDAMED
Model / Reference
STRETCHERS EUDAMED
870.04 EUDAMED

Identifiers

Primary DI / UDI-DI
08023577045573 EUDAMED
Basic UDI-DI
8023577STRETCHERSQP EUDAMED
Direct Marketing DI
08023577045573 EUDAMED
EMDN Code
V08050199 PATIENT TRANSFER STRETCHERS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Lecco X-Large by KONG S.p.A. — 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

Manufacturer
KONG S.p.A.
EUDAMED SRN
IT-MF-000027905

Sources (1)

  • EUDAMED b0ff31ee-c806-4c91-99d7-fe56538ed1a9 61 fields · synced Jul 13, 2026