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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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PES Instruments — 12 UDI-DI variants, MDR (MedXpert GmbH)

MD Atlas
MedXpert GmbH

Data from EUDAMED, last updated May 23, 2026

PES Instruments

426002958MEDXPERT-PESB5A

12 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: MedXpert GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426002958MEDXPERT-PESB5A
Device name: PES Instruments
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: MedXpert GmbH
SRN: DE-MF-000005489
Country: Germany
Email: ask-the-xpert@medxpert.de
Phone: +49 76345085630

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01KFN7K3CWQN0DQYT5GNJ8VK3X

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

021-0922904260029580259
021-1127904260029580273
021-1743204260029580334
021-0820304260029580242
021-1333004260029580297
020-0002204260029580136
021-1435604260029580303
021-16406 04260029580327
021-1025404260029580266
021-1230504260029580280
021-0717804260029580235
021-1538104260029580310