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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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Bisswälle — 6 UDI-DI variants, MDR (al dente Dentalprodukte GmbH)

MD Atlas
al dente Dentalprodukte GmbH

Data from EUDAMED, last updated May 23, 2026

Bisswälle

426253316BiteRimC6

6 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: al dente Dentalprodukte GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426253316BiteRimC6
Device name: Bisswälle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: al dente Dentalprodukte GmbH
SRN: DE-MF-000005029
Country: Germany
Email: info@aldente.de
Phone: +49(0)5321-80031

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JWR96PBVN3QKZ884NCYC2E35

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

MUSTER02-421004262533160262
MUSTER02-420004262533160255
02-421004262533160118
02-420004262533160101
02-422004262533160125
MUSTER02-422004262533160279