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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 Tulip sleeve — 3 UDI-DI variants, MDR

MD Atlas
Paradigm Spine GmbH

Data from EUDAMED, last updated May 23, 2026

HPS™ 2.0 MIS Tulip sleeve

0426014889003-031X3

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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0426014889003-031X3
Device name: HPS™ 2.0 MIS Tulip sleeve
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 24, 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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Applied filters

basicUdiUlid01KJ896SK4GPG1SZSA2V5WN6RS

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

HBT6041004260636672460
HBT6030004260148899669
HBT6040004260148899676