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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

I.T.A. — Class I MDR by Sympatient GmbH

MD Atlas
Sympatient GmbH

EUDAMED last updated this device on Apr 21, 2026

I.T.A.

PP12332I.T.A.74

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Sympatient GmbH
UDI-DI code: 1312332I.T.A.002023
Reference / catalog number: I.T.A.

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Manufacturer information

Organization name: Sympatient GmbH
SRN: DE-MF-000019383
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW030
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 1312332I.T.A.002023
Basic UDI-DI: PP12332I.T.A.74
Reference / catalog number: I.T.A.
Issuing entity: IFA

Classification

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

Device details

Quantity: 1
Additional product description: "Invirto - Die Therapie gegen Angst" is a medical device system that includes a software application and a VR headset. The medical device system provides patients with psychotherapeutic information and strategies allowing them self-managed, location-independent treatment of psychological disorders (e.g. anxiety disorders) to reduce the disorders symptoms.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

I.T.DPP12332I.D88On the market I.T.A.PP12332I.T.A.74On the market I.A.A.PP12332I.A.A.59On 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.