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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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Eindrehinstrumente (Insertion… — 4 UDI-DI variants, MDR

MD Atlas
surgebright GmbH

Data from EUDAMED, last updated May 23, 2026

Eindrehinstrumente (Insertion Instruments)

9120125220014E

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: surgebright GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 9120125220014E
Device name: Eindrehinstrumente (Insertion Instruments)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: surgebright GmbH
SRN: AT-MF-000002664
Country: Austria
Email: info@surgebright.com
Phone: +43 720 371 355

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GM7ZGY99YH2VJEQ9EFV02D3C

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

Shark Screw® coupling09120125220037
Shark Screw® driver acl09120125220259
Shark Screw® driver cut09120125220242
Shark Screw® driver ht09120125220266