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Forced-air hot air sterilizers

EUDAMED

Class IIb (EU MDR)

Ref A3-214-535VModel Forced-air hot air sterilizers

by Titanox S.r.l.

Identity

Device Name
Forced-air hot air sterilizers EUDAMED
Model / Reference
Forced-air hot air sterilizers EUDAMED
A3-214-535V EUDAMED

Identifiers

Primary DI / UDI-DI
08059304700064 EUDAMED
Basic UDI-DI
805930470A06VENTFORZZ4 EUDAMED
EMDN Code
Z12011307 DRY AIR STERILISERS 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

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

Forced-air hot air sterilizers by Titanox S.r.l. — Class IIb — 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
Titanox S.r.l.
EUDAMED SRN
IT-MF-000020325

Sources (1)

  • EUDAMED e840e122-ecb3-4a25-b64a-bdae77825b3d 61 fields · synced Jul 11, 2026