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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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Planeringstavla — 6 UDI-DI variants, MDR

MD Atlas
LVI Low Vision International AB

Data from EUDAMED, last updated May 31, 2026

Planeringstavla

7330724PBSL

6 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7330724PBSL
Device name: Planeringstavla
Device model: Plannerboard
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 12, 2026

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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KH8P9X4YVGTCZXHTXM4WS0WN

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

PB-D07330724005597
PB-D-Mi07330724005603
PB-W07330724005559
PB-W-C07330724005573
PB-W-Mi07330724005566
PB-W-Mi-C07330724005580