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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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phenox Detachment Cable — 2 UDI-DI variants, MDR (phenox GmbH)

MD Atlas
phenox GmbH

Data from EUDAMED, last updated May 23, 2026

phenox Detachment Cable

426012378DetachementCabHN

2 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: phenox GmbH

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 1000266807
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Nov 20, 2025 → Dec 20, 2028

Identity & classification

Basic UDI-DI: 426012378DetachementCabHN
Device name: phenox Detachment Cable
Device model: Neurovascular Treatment Accessories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 24, 2023

Manufacturer & authorised representative

Manufacturer

Name: phenox GmbH
SRN: DE-MF-000006524
Country: Germany
Email: info@phenox.info
Phone: +49234369190

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GY9RZH8FQH2JTAB5QDQFQX9M

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

PDC-NRC04260123784812
PDC-RC04260123784805