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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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PROGNOST XPE — 10 UDI-DI variants, MDR (PROTEC X-ray Systems GmbH)

MD Atlas
PROTEC X-ray Systems GmbH

Data from EUDAMED, last updated May 23, 2026

PROGNOST XPE

426050264X011ZE

10 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: PROTEC X-ray Systems GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426050264X011ZE
Device name: PROGNOST XPE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: PROTEC X-ray Systems GmbH
SRN: DE-MF-000048351
Country: Germany
Email: info@protec-med.com
Phone: +49 7062 9255 0

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQT9X5Q2QZAN0D8V70SEVWVJ

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

7037-6-171204260502640272
7037-1-171304260502641828
7037-1-171404260502641835
7037-6-171404260502640296
7037-6-171104260502640265
7037-1-171004260502641798
7037-1-171204260502641811
7037-6-171304260502640289
7037-6-171004260502640258
7037-1-171104260502641804