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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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SpineQ — 2 UDI-DI variants, MDR (Bonescreen GmbH)

MD Atlas
Bonescreen GmbH

Data from EUDAMED, last updated May 23, 2026

SpineQ

426247034BS00001QE

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: Bonescreen GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426247034BS00001QE
Device name: SpineQ
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: Bonescreen GmbH
SRN: DE-MF-000036576
Country: Germany
Email: jan.kirschke@bonescreen.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J5D2R38WE9XAW377FT248TXE

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

SpineQ v1.3.004262470340031
SpineQ v1.2.004262470340024