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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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Storage trays — 38 UDI-DI variants, MDR (Peter Lazic GmbH)

MD Atlas
Peter Lazic GmbH

Data from EUDAMED, last updated May 23, 2026

Storage trays

42506037-1-0-CI01-C01-E7

38 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-C01-E7
Device name: Storage trays
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

38 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS4VEZZV9A802T9YMSD9CCD3

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

64.020.1504250603743125
35.02604250603743798
56.02204250603743842
64.020.1104250603743200
19.102.0104250603744801
46.02504250603712633
35.02804250603746522
64.021.1004250603743217
64.020.0204250603734840
19.104.0104250603746997
46.690.2004250603743927
64.999.0204250603743149
64.020.1204250603743194

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