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VitaGuard VG 5 PX

EUDAMED

Class IIb (EU MDR)

Ref 73213013Model VitaGuard VG 5

by GETEMED Medizin- und Informationstechnik AG

Identity

Trade Name
VitaGuard VG 5 PX EUDAMED
Device Name
VitaGuard VG 5 EUDAMED
Model / Reference
VitaGuard VG 5 EUDAMED
73213013 EUDAMED

Identifiers

Primary DI / UDI-DI
04250903200199 EUDAMED
Basic UDI-DI
0425090320239NH EUDAMED
Direct Marketing DI
04250903200199 EUDAMED
EMDN Code
Z1203020202 TRANSPORTABLE/PORTABLE MULTI–PARAMETER PATIENT MONITORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

VitaGuard VG 5 PX by Getemed Medizin- Und Informationstechnik Ag — 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

EUDAMED SRN
DE-MF-000012384

Sources (1)

  • EUDAMED 322cf96a-b112-4faa-ab7a-6b23be1ae4f0 61 fields · synced Jul 20, 2026