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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

Careable — Class I MDR by Careable Labs AB

MD Atlas
Careable Labs AB

EUDAMED last updated this device on May 12, 2026

Careable

735018823CARHP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Careable Labs AB
UDI-DI code: 07350188230014
Reference / catalog number: Careable

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View device family (Basic UDI)

Manufacturer information

Organization name: Careable Labs AB
SRN: SE-MF-000054068
Manufacturer status: Active

Critical warnings

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

CW018
For non-emergency use only

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement	May 18, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07350188230014
Basic UDI-DI: 735018823CARHP
Reference / catalog number: Careable
Issuing entity: GS1

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: Careable är en molnbaserad SaaS-plattform som stödjer insamling, strukturering och dokumentation av patientrapporterad information inom triageprocessen för icke-akut hälso- och sjukvård. Systemet effektiviserar arbetsflödet från inkommande samtal till färdig journalanteckning. Careable fattar inte kliniska triagebeslut.
Additional information URL: https://docs.careable.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

Encoded

(01)07350188230014

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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

This device is not currently linked to any other device.

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.