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X-Trim 2.0

EUDAMED

Class I (EU MDR)

Ref 855.16Model SPINALB

by KONG S.p.A.

Identity

Trade Name
X-TRIM 2.0 EUDAMED
Model / Reference
SPINALB EUDAMED
855.16 EUDAMED

Identifiers

Primary DI / UDI-DI
08023577075396 EUDAMED
Basic UDI-DI
8023577SPINALB5S EUDAMED
Direct Marketing DI
08023577075396 EUDAMED
EMDN Code
V080504 PATIENT TRANSFER BOARDS AND TABLES 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

Category: Patient lifting system stretcher

X-Trim 2.0 by KONG S.p.A. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Patient lifting system stretcher.

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 55883d71-9772-4048-8bfc-905d597a8a8e 61 fields · synced Jul 28, 2026