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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

Mindable: Social Phobia — Class I MDD by Mindable Health GmbH

MD Atlas
Mindable Health GmbH

EUDAMED last updated this device on May 27, 2026

Mindable: Social Phobia

B-SPA-v2.x.xUB

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Mindable Health GmbH
UDI-DI code: D-SPA-v2.x.xUB
Reference / catalog number: Mindable: Social Phobia

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View device family (Basic UDI)

Manufacturer information

Organization name: Mindable Health GmbH
SRN: DE-MF-000006593
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Contraindications: The application is not allowed to be used in case of suicidal risk or acute self-injurious tendencies.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Sep 2, 2022	Still on market

Device identification

Trade name: Mindable: Social Phobia
UDI-DI code: D-SPA-v2.x.xUB
Basic UDI-DI: B-SPA-v2.x.xUB
Reference / catalog number: Mindable: Social Phobia
Issuing entity: EUDAMED

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: —
Additional information URL: https://www.mindable.health/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

D-SPA-v2.x.xUB

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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Related devices

Mindable: Panic & AgoraphobiaB-PDA-v1.x.xGMOn 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.