← Back to catalogue

Lecco 2.0

EUDAMED

Class I (EU MDR)

Ref 870.04Model STRETCHERS

by KONG S.p.A.

Identity

Trade Name
LECCO 2.0 EUDAMED
Model / Reference
STRETCHERS EUDAMED
870.04 EUDAMED

Identifiers

Primary DI / UDI-DI
08023577058580 EUDAMED
Basic UDI-DI
8023577STRETCHERSQP EUDAMED
Direct Marketing DI
08023577058580 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 2.0 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

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

Manufacturer

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

Sources (1)

  • EUDAMED 4cb83590-f08e-4384-ab8a-93226cda241c 61 fields · synced Jun 19, 2026