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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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Osteotom — 2 UDI-DI variants, MDR (Noris Medical GmbH)

MD Atlas
Noris Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Osteotom

426069822Osteotom1ZM

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Noris Medical GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 426069822Osteotom1ZM
Device name: Osteotom
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Noris Medical GmbH
SRN: DE-MF-000022591
Country: Germany
Email: katya@norismedical.com
Phone: +972528011918

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRXP6Q1XHRA17QNY2E6HX9SR

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

NG-X300104260698228322
NG-X300204260698228339