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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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Kamerasystem — 4 UDI-DI variants, MDR

MD Atlas
LVI Low Vision International AB

Data from EUDAMED, last updated May 31, 2026

Kamerasystem

7330724MLZES

4 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: LVI Low Vision International AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7330724MLZES
Device name: Kamerasystem
Device model: ML-ZIP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: LVI Low Vision International AB
SRN: SE-MF-000004178
Country: Sweden
Email: info@lvi.se
Phone: +46470727700

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K4QCPA0QPCMJQ723KQV3SHGB

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

MLZ-FHD1307330724005399
MLZ-FHD13-A07330724005375
MLZ-FHD1707330724005382
MLZ-FHD17-A07330724005368