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Inthes

EUDAMED

Class I (EU MDR)

Ref 320832Model 320740, 320750, 320750RX, 320830_E, 320832, 320834, 320760RX, 320760, 320610R

by Malvestio Spa

Identity

Trade Name
INTHES EUDAMED
Device Name
AGILE, BRERA, ENTHES, INTHES, ITALA, SISTY EUDAMED
Model / Reference
320740, 320750, 320750RX, 320830_E, 320832, 320834, 320760RX, 320760, 320610R EUDAMED
320832 EUDAMED

Identifiers

Primary DI / UDI-DI
08058302600222 EUDAMED
Basic UDI-DI
805830260BARMEC66 EUDAMED
Direct Marketing DI
08058302600222 EUDAMED
EMDN Code
V08050101 GENERIC USE STRETCHERS 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

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

Inthes by Malvestio Spa — 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
Malvestio Spa
EUDAMED SRN
IT-MF-000013307

Sources (1)

  • EUDAMED 07b0159e-2afe-46e6-88a7-86ebd053c5d4 61 fields · synced Jun 18, 2026