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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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KPFF26V KPFF 52V — 2 UDI-DI variants, MDR

MD Atlas
KW Apparecchi Scientifici Srl

Data from EUDAMED, last updated May 31, 2026

KPFF26V KPFF 52V

805750615AB002XV

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: KW Apparecchi Scientifici Srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805750615AB002XV
Device name: —
Device model: KPFF26V KPFF 52V
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: KW Apparecchi Scientifici Srl
SRN: IT-MF-000029722
Country: Italy
Email: s.ingrande@kwkw.it
Phone: +39 0577309143

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSN0H4BG3V6E93T5NNF9GE4P

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

RAPID PLASMA FREEZER08057506152117
RAPID PLASMA FREEZER08057506152100