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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

RAPID PLASMA FREEZER — Class IIa MDR by KW Apparecchi…

MD Atlas
KW Apparecchi Scientifici Srl

EUDAMED last updated this device on May 27, 2026

RAPID PLASMA FREEZER

805750615AB002XV

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: KW Apparecchi Scientifici Srl
UDI-DI code: 08057506152100
Reference / catalog number: KPFF26V

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View device family (Basic UDI)

Manufacturer information

Organization name: KW Apparecchi Scientifici Srl
SRN: IT-MF-000029722
Manufacturer status: Active

Critical warnings

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

CW263
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW018
EUDAMED did not publish a description for this code.
CW071
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jul 13, 2026	Still on market

Device identification

Trade name: RAPID PLASMA FREEZER
UDI-DI code: 08057506152100
Basic UDI-DI: 805750615AB002XV
Reference / catalog number: KPFF26V
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: —
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

UDI-DI DataMatrix

Encoded

(01)08057506152100

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Z121702BLOOD AND BLOOD COMPONENTS FREEZERS

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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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.