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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

v4.2.0 — Class I MDD by ifap Service-Institut…

MD Atlas
ifap Service-Institut für Ärzte und Apotheker GmbH

EUDAMED last updated this device on Jan 19, 2026

v4.2.0

B-1311682TFMEDSCORES4.283

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ifap Service-Institut für Ärzte und Apotheker GmbH
UDI-DI code: 1311682TFMEDSCORES4.283
Reference / catalog number: v4.2.0

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Manufacturer information

Organization name: ifap Service-Institut für Ärzte und Apotheker GmbH
SRN: DE-MF-000006908
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 1311682TFMEDSCORES4.283
Basic UDI-DI: B-1311682TFMEDSCORES4.283
Reference / catalog number: v4.2.0
Issuing entity: IFA

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Das Medizinprodukt GHG Praxisdienst Medizinische Scores dient dem fachkundigen Arzt als Hilfsmittel zur Berechnung medizinischer Scores und kann vom Arzt in der Behandlungssituation als Entscheidungsunterstützung dienen. Dazu werden die Eingaben des Vertragspartners verschlüsselt an einen Server der ifap übertragen, auf dem die Berechnung der Score-Werte stattfindet. Anfrageparameter und Berechnungsergebnisse werden mit einem Zeitstempel anonymisiert gespeichert. Ohne Internetverbindung kann das Modul GHG Praxisdienst Medizinische Scores nicht verwendet werden.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12040292GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.