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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

CC01.I — Class I MDR by QWINCE INNOVATION S.R.L.

MD Atlas
QWINCE INNOVATION S.R.L.

EUDAMED last updated this device on Dec 5, 2025

CC01.I

805689734.Farma23PZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: QWINCE INNOVATION S.R.L.
UDI-DI code: 08056897340028
Reference / catalog number: CC01.I

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View device family (Basic UDI)

Manufacturer information

Organization name: QWINCE INNOVATION S.R.L.
SRN: IT-MF-000029688
Manufacturer status: Active

Related devices

PF01.II805689734.FARMA24RLOn the market PF01.I805689734.Farma23PZOn the market PFF01.II805689734.FARMA24RLOn the market CC01.II805689734.FARMA24RLOn the market DF01.I805689734.Farma23PZOn 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08056897340028
Basic UDI-DI: 805689734.Farma23PZ
Reference / catalog number: CC01.I
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: ConCura è un dispositivo medico per acquisire, salvare, visualizzare e trasferire dati rilevanti per la presa in carico del paziente cronico e per favorire comportamenti orientati all’aderenza alle terapie mediante servizio di supporto e monitoraggio di personale specializzato
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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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