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Neudry

EUDAMED

Class I (EU MDR)

Ref 116

by Biodisin S.r.l

Identity

Trade Name
Neudry EUDAMED
Device Name
Neudry EUDAMED
Model / Reference
116 EUDAMED

Identifiers

Primary DI / UDI-DI
08055712800563 EUDAMED
Basic UDI-DI
805571280Neudry8G EUDAMED
EMDN Code
Z12011385 CLEANING, DISINFECTION AND STERILISATION INSTRUMENTS - CONSUMABLES 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

Neudry by Biodisin S.r.l — 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
Biodisin S.r.l
EUDAMED SRN
IT-MF-000031661

Sources (1)

  • EUDAMED 69474d09-2443-4fce-8f78-9c870ce6a4d4 61 fields · synced Jun 19, 2026