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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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Elektrodenbezüge — 17 UDI-DI variants, MDR

MD Atlas
Lazina med elektrodenservice

Data from EUDAMED, last updated May 23, 2026

Elektrodenbezüge

426062852BZRJ

17 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: Lazina med elektrodenservice

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426062852BZRJ
Device name: Elektrodenbezüge
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: Lazina med elektrodenservice
SRN: DE-MF-000005288
Country: Germany
Email: admin@Lazina.com
Phone: 045239846813

Variants by status

UDI-DI variants

17 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRVGMR6HYA825JVRXHGVVPHA

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

01004260628520106
01204260628520120
01504260628520151
01604260628520168
02004260628520205
02104260628520212
02504260628520250
02604260628520267
03004260628520304
03304260628520335
03504260628520359
06004260628520601
06204260628520625
05004260628520502
05104260628520519
06104260628520618
03104260628520311