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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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Nasal specula — 17 UDI-DI variants, MDR (Peter Lazic GmbH)

MD Atlas
Peter Lazic GmbH

Data from EUDAMED, last updated May 23, 2026

Nasal specula

42506037-1-0-CI01-N01-GL

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: Peter Lazic GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42506037-1-0-CI01-N01-GL
Device name: Nasal specula
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

17 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS4VJ3HPD696BSPX6J8BFK16

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

70.592.0104250603738794
70.595.0304250603738756
70.592.0304250603738817
70.592.0504250603738831
70.592.0704250603738855
70.592.0604250603738848
70.581.0104250603738718
70.592.0404250603738824
70.581.0204250603742036
70.581.0404250603738725
70.589.0104250603738763
70.589.0204250603738770
70.581.0304250603741688
70.592.0204250603738800
70.595.0204250603738749
70.595.0104250603738084
70.589.0304250603738787