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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 — 4 UDI-DI variants, MDR (Yeti Dentalprodukte GmbH)

MD Atlas
Yeti Dentalprodukte GmbH

Data from EUDAMED, last updated May 23, 2026

Bisswälle

42518578BissregWallG3

4 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: Yeti Dentalprodukte GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42518578BissregWallG3
Device name: Bisswälle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 7, 2021

Manufacturer & authorised representative

Manufacturer

Name: Yeti Dentalprodukte GmbH
SRN: DE-MF-000005557
Country: Germany
Email: qm@yeti-dental.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FHCT4QX7BXWFQJG4TTCMNSRN

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

610-0100+EYET6100100
612-0100+EYET6120100
613-0100+EYET6130100
611-0100+EYET6110100