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Negavent T 230

EUDAMED

Class IIb (EU MDR)

Ref NV21

by Dima Italia S.r.l.

Identity

Trade Name
NEGAVENT T 230 EUDAMED
Device Name
Negavent T 230 EUDAMED
Model / Reference
NV21 EUDAMED

Identifiers

Primary DI / UDI-DI
08058647920535 EUDAMED
Basic UDI-DI
B-08058647920535 EUDAMED
EMDN Code
Z1203019099 VARIOUS INSTRUMENTS FOR ANAESTHESIA AND PULMONARY VENTILATION SUPPORT – OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Negavent T 230 by Dima Italia S.r.l. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Dima Italia S.r.l.
EUDAMED SRN
IT-MF-000020327

Sources (1)

  • EUDAMED e81c4324-320d-4d5a-b2d1-765ced329239 61 fields · synced Jun 18, 2026