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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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HF cable — 16 UDI-DI variants, MDR (Peter Lazic GmbH)

MD Atlas
Peter Lazic GmbH

Data from EUDAMED, last updated May 23, 2026

HF cable

42506037-1-0-CI01-Z02-KB

16 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: Peter Lazic GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42506037-1-0-CI01-Z02-KB
Device name: HF cable
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Peter Lazic GmbH
SRN: DE-MF-000005519
Country: Germany
Email: eudamed@lazic.de
Phone: +49 7461 96643 0

Variants by status

UDI-DI variants

16 UDI-DI variants

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Applied filters

basicUdiUlid01KS4VKZQTTGP8QS5ZYRNYV5DK

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

69.451.3004250603720942
69.481.3104250603730385
69.471.5004250603721062
69.471.5104250603730378
69.471.3104250603730361
69.451.3104250603730330
69.461.5004250603721048
69.451.5104250603730347
69.481.3004250603721079
69.481.5104250603730392
69.461.3004250603721031
69.451.5004250603721024
69.461.3104250603730323
69.481.5004250603721086
69.471.3004250603721055
69.461.5104250603730354