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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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Manual wheelchair — 1 UDI-DI variant, MDD (M Prekyba UAB)

MD Atlas
M Prekyba UAB

Data from EUDAMED, last updated May 30, 2026

Manual wheelchair

B-04779054140104

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: M Prekyba UAB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-04779054140104
Device name: Manual wheelchair
Device model: SATURN XL
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Jul 15, 2024

Manufacturer & authorised representative

Manufacturer

Name: M Prekyba UAB
SRN: LT-MF-000022623
Country: Lithuania
Email: info@mprekyba.lt
Phone: +37069889208

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J2V759M5TFKWWAGJTZWXJYY9

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

SATURN XL04779054140104