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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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HPS™ 2.0 MIS Screw Blade remover — 3 UDI-DI variants, MDR

MD Atlas
Paradigm Spine GmbH

Data from EUDAMED, last updated May 23, 2026

HPS™ 2.0 MIS Screw Blade remover

0426014889003-021WY

3 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: Paradigm Spine GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 0426014889003-021WY
Device name: HPS™ 2.0 MIS Screw Blade remover
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Paradigm Spine GmbH
SRN: DE-MF-000011231
Country: Germany
Email: franz.menean@medagent.de
Phone: +49746399540

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KHR5CHNX8DWHY0W6V54WF69E

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

HBT9029604260148899805
HBT9029404260148899966
HBT9029004260148899768