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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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Probe Navigator — 5 UDI-DI variants, MDR (Z-Medical GmbH + Co. KG)

MD Atlas
Z-Medical GmbH + Co. KG

Data from EUDAMED, last updated May 23, 2026

Probe Navigator

4057217PROBENAVIGATORXT

5 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: Z-Medical GmbH + Co. KG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 4057217PROBENAVIGATORXT
Device name: Probe Navigator
Device model: Probe Navigator
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: Z-Medical GmbH + Co. KG
SRN: DE-MF-000005471
Country: Germany
Email: info@z-medical.de

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01JEDFMQ3HRA9PCX6FEZ51KRW4

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

Probe Navigator04057217006093
Probe Navigator bayonet04057217006123
Probe Navigator bayonet04057217006116
Probe Navigator straight04057217006109
Rack04057217006130