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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

PF01.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

PF01.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: 08056897340011
Reference / catalog number: PF01.I

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Manufacturer information

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

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: 08056897340011
Basic UDI-DI: 805689734.Farma23PZ
Reference / catalog number: PF01.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: PuntoFarma 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.
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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Related devices

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