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Ixosafe

EUDAMED

Class I (EU MDR)

Ref 2791

by ALFA VITA, s.r.o.

Identity

Trade Name
IXOSAFE EUDAMED
Device Name
IXOSAFE EUDAMED
Model / Reference
2791 EUDAMED

Identifiers

Primary DI / UDI-DI
08594027313790 EUDAMED
Basic UDI-DI
859402731001GP EUDAMED
Direct Marketing DI
08594027313790 EUDAMED
EMDN Code
V901099 PARASITE ELIMINATION MECHANICAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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

Ixosafe by ALFA VITA, s.r.o. — 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
ALFA VITA, s.r.o.
EUDAMED SRN
CZ-MF-000051941

Sources (1)

  • EUDAMED 61e53ab5-c4d0-4cad-b291-28cdeb135d37 61 fields · synced Jun 19, 2026