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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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AquaBella Duschschutzfolie — 14 UDI-DI variants, MDR

MD Atlas
AquaBella, Christian Dontenvill

Data from EUDAMED, last updated May 23, 2026

AquaBella Duschschutzfolie

40383840000176

14 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: AquaBella, Christian Dontenvill

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40383840000176
Device name: AquaBella Duschschutzfolie
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: AquaBella, Christian Dontenvill
SRN: DE-MF-000006424
Country: Germany
Email: info@medi-help.de
Phone: +49 731 60 227 08

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPQK1X3S30QSQZ2KWK48R6RB

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

A04038384124100
AquaBella04038384123547
AquaBella04038384123653
C04038384124322
AquaBella04038384123325
AquaBella04038384123431
D 04038384124438
I04038384124650
AquaBella04038384123219
AquaBella04038384123103
D Junior04038384124766
K04038384124544
AquaBella04038384123769
B04038384124216