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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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HexaFilt — 3 UDI-DI variants, MDR (eXagotec GmbH)

MD Atlas
eXagotec GmbH

Data from EUDAMED, last updated May 23, 2026

HexaFilt

426251068HFPH

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: eXagotec GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426251068HFPH
Device name: HexaFilt
Device model: 11000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: eXagotec GmbH
SRN: DE-MF-000046512
Country: Germany
Email: qmre@exagotec.com
Phone: +491733571907

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JW68975TGKRW2K2G45EG9ZHT

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

1100004262510680004
1101004262510680028
HexaFilt®04262510680035