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Ηλεκτρικός Γερανός Ανύψωσης

EUDAMED

Class I (EU MDR)

Ref 058.00522

by Χριστοφορος Κυφιδης Και Σια Ε.ε.

Identity

Trade Name
Ηλεκτρικός Γερανός Ανύψωσης EUDAMED
Device Name
Συσκευές Ανύψωσης Ατόμων EUDAMED
Model / Reference
058.00522 EUDAMED

Identifiers

Primary DI / UDI-DI
05210077043434 EUDAMED
Basic UDI-DI
5210077LiftDevicesC4 EUDAMED
Direct Marketing DI
05210077043434 EUDAMED
EMDN Code
V0805030102 ELECTRIC MOBILE LIFTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Ηλεκτρικός Γερανός Ανύψωσης by Χριστοφορος Κυφιδης Και Σια Ε.ε. — 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

EUDAMED SRN
GR-MF-000023673

Sources (1)

  • EUDAMED f726c234-89ed-4594-84d3-9d8e78b9710b 61 fields · synced Jul 9, 2026