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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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Drill Stoppers — 6 UDI-DI variants, MDR (Noris Medical GmbH)

MD Atlas
Noris Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Drill Stoppers

426069822Stopper1Y9

6 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: 426069822Stopper1Y9
Device name: Drill Stoppers
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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRXMFYQGFADSWNRFNW7GCGNM

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

NGSD732004260698229459
NGSD732504260698229473
NGSD732204260698229466
NGSD731804260698229442
NGSD251004260698229435
NGSD781104260698229084