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Electronic Pasteur hot air sterilizers

EUDAMED

Class IIb (EU MDR)

Ref A3-218-670Model Electronic Pasteur hot air sterilizers

by Titanox S.r.l.

Identity

Device Name
Electronic Pasteur hot air sterilizers EUDAMED
Model / Reference
Electronic Pasteur hot air sterilizers EUDAMED
A3-218-670 EUDAMED

Identifiers

Primary DI / UDI-DI
08059304700101 EUDAMED
Basic UDI-DI
805930470A06PASTELTNCMD 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

Electronic Pasteur 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 8ca35ff3-2eb8-4112-8a03-d2ec2a426d8d 61 fields · synced Jul 14, 2026