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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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Bissnehmewachs in Stangen — 6 UDI-DI variants, MDR (Karl Berg GmbH)

MD Atlas
Karl Berg GmbH

Data from EUDAMED, last updated May 23, 2026

Bissnehmewachs in Stangen

426075024BissRegCM

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: Karl Berg GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426075024BissRegCM
Device name: Bissnehmewachs in Stangen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 6, 2021

Manufacturer & authorised representative

Manufacturer

Name: Karl Berg GmbH
SRN: DE-MF-000005811
Country: Germany
Email: qm@yeti-dental.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01FHASSEJM8P1FNFNKQJNZDRNF

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

40001+EBER40001
40000+EBER40000
40003+EBER40003
40002+EBER40002
40007+EBER40007
40006+EBER40006