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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

R5.1 — Class IIa MDR by ifap Service-Institut…

MD Atlas
ifap Service-Institut für Ärzte und Apotheker GmbH

EUDAMED last updated this device on Feb 18, 2026

R5.1

PP11682TFPROMEDSCORESR565

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ifap Service-Institut für Ärzte und Apotheker GmbH
UDI-DI code: 1311682TFMEDSCORES5.181
Reference / catalog number: R5.1

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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.

Country	On market since	Until
GermanyPrimary placement	Feb 13, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 1311682TFMEDSCORES5.181
Basic UDI-DI: PP11682TFPROMEDSCORESR565
Reference / catalog number: R5.1
Issuing entity: IFA

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Das Modul THERAFOX PRO Medical Scores (alternativ in Kurzform “TF PRO MedScores” oder “Medical Scores” genannt) dient als Entscheidungsunterstützung bei der Diagnose, Verhütung, Überwachung, Vorhersage und Behandlung durch medizinische Scores, die von qualifizierten Ärzten sowie anderem medizinischen Fachpersonal 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

Related devices

ab R4.1B-1311682TFMEDSCORES4.161On the market THERAFOX PRO AMTS ab R5.0PP11682THERAFOXPRO60On the market v4.2.0B-1311682TFMEDSCORES4.283On the market

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.