Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

EHL-Probe — 9 UDI-DI variants, MDR (Walz Elektronik GmbH)

MD Atlas
Walz Elektronik GmbH

Data from EUDAMED, last updated May 23, 2026

EHL-Probe

426066754EHL-PROBE6M

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Walz Elektronik GmbH

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426066754EHL-PROBE6M
Device name: EHL-Probe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 30, 2022

Manufacturer & authorised representative

Manufacturer

Name: Walz Elektronik GmbH
SRN: DE-MF-000006132
Country: Germany
Email: info@walz-el.de
Phone: +49 7452 2020

Variants by status

UDI-DI variants

9 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01FTNRB0F6NSVFTXPWM0JSEVYY

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

P201400FST04260667540035
P30950FST04260667540110
P453000FST04260667540196
P303000FST04260667540158
P243000FST04260667540097
P70450FST04260667540219
P303000SST04260667540134
P45600FST04260667540172
P243000SST04260667540059