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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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Alcohol Based Disinfection Wipes — 128 UDI-DI variants, MDR

MD Atlas
BABGENCEL GmbH

Data from EUDAMED, last updated May 23, 2026

Alcohol Based Disinfection Wipes

426071005HW0000000RV

128 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: BABGENCEL GmbH

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: MDR00145-A
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: Jun 12, 2025 → Feb 3, 2030

Identity & classification

Basic UDI-DI: 426071005HW0000000RV
Device name: Alcohol Based Disinfection Wipes
Device model: 20HW01 / 20HW02
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: BABGENCEL GmbH
SRN: DE-MF-000019691
Country: Germany
Email: info@babgencel.de
Phone: +49 211 90981888

Variants by status

UDI-DI variants

128 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRDMH6PVH820ZADGSEAHGF51

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

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