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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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Biss-Stangen — 7 UDI-DI variants, MDR

MD Atlas
SILADENT Dr. Böhme & Schöps GmbH

Data from EUDAMED, last updated May 31, 2026

Biss-Stangen

42559118BiteStickAR

7 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: SILADENT Dr. Böhme & Schöps GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42559118BiteStickAR
Device name: —
Device model: Biss-Stangen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: SILADENT Dr. Böhme & Schöps GmbH
SRN: DE-MF-000052689
Country: Germany
Email: info@siladent.de
Phone: +49532137790

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSSEA2ZPTCGWQZSE5P6G12WP

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

C02-426004255911800218
02-426004255911800140
02-426504255911800157
C02-425504255911800201
02-425504255911800133
MUSTER02-426004255911800294
MUSTER02-425504255911800287