← Back to catalogue

ReSTA

EUDAMED

Class I (EU MDR)

Ref 75313011Model ReSTA

by GETEMED Medizin- und Informationstechnik AG

Identity

Trade Name
ReSTA EUDAMED
Device Name
ReSTA EUDAMED
Model / Reference
ReSTA EUDAMED
75313011 EUDAMED

Identifiers

Primary DI / UDI-DI
04250903202575 EUDAMED
Basic UDI-DI
0425090320269NS EUDAMED
EMDN Code
Z12050492 HOLTER SYSTEM INSTRUMENTS FOR CARDIOVASCULAR PARAMETERS - MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class I 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

ReSTA by Getemed Medizin- Und Informationstechnik Ag — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000012384

Sources (1)

  • EUDAMED 051c40ad-19ec-474e-b5a0-37bca6d02137 61 fields · synced Jun 18, 2026