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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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Leyla retractor — 12 UDI-DI variants, MDR (Peter Lazic GmbH)

MD Atlas
Peter Lazic GmbH

Data from EUDAMED, last updated May 23, 2026

Leyla retractor

42506037-1-0-CI01-Z03-KE

12 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-Z03-KE
Device name: Leyla retractor
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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS4VMQCMEHVJ7G85ACP4H2FQ

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

70.280.0204250603736479
70.268.0204250603735823
70.282.0204250603736486
70.275.0204250603736462
70.266.0204250603736431
70.273.0204250603735847
70.284.0204250603736509
70.274.0204250603736455
70.267.0204250603736448
70.283.0204250603736493
70.285.0204250603736516
70.270.0204250603735830