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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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KWAP24 KWAP18 KWAP48 KWAP54 KWAP96… — 7 UDI-DI variants, MDR

MD Atlas
KW Apparecchi Scientifici Srl

Data from EUDAMED, last updated May 31, 2026

KWAP24 KWAP18 KWAP48 KWAP54 KWAP96 KWAP108 KWAP180

805750615AG001YW

7 UDI-DI variants

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805750615AG001YW
Device name: —
Device model: KWAP24 KWAP18 KWAP48 KWAP54 KWAP96 KWAP108 KWAP180
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KRKK2QSMKW1Y64E6FBRRPMDG

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

PLATELET AGITATOR - KWAP08057506150854
KWAP4808057506150069
KWAP9608057506150083
KWAP18008057506150106
KWAP5408057506150076
KWAP1808057506150052
KWAP10808057506150090