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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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LUMBOSACRAL SPINE ORTHOSES — 7 UDI-DI variants, MDR

MD Atlas
medi GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

LUMBOSACRAL SPINE ORTHOSES

4026398Y060308034B

7 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: medi GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4026398Y060308034B
Device name: LUMBOSACRAL SPINE ORTHOSES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: medi GmbH & Co. KG
SRN: DE-MF-000007092
Country: Germany
Email: info@medi.de

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2YD8T2T15MF5BWPHXC6SPK

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

K29020200004068903554248
K29020100004068903554231
K29020700004068903554293
K29020300004068903554255
K29020500004068903554279
K29020400004068903554262
K29020600004068903554286