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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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Wózek medyczny — 1 UDI-DI variant, MDD (ABINOX Piotr Szłapka)

MD Atlas
ABINOX Piotr Szłapka

Data from EUDAMED, last updated May 30, 2026

Wózek medyczny

B-59069357990552

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: ABINOX Piotr Szłapka

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-59069357990552
Device name: Wózek medyczny
Device model: 2-001, 2-002, 2-003, 2-005, 2-006, 2-007, 2-008, 2-009, 2-010, 2-011, 2-015, 2-016
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: ABINOX Piotr Szłapka
SRN: PL-MF-000043281
Country: Poland
Email: office@abinox.eu
Phone: +48501342416

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSMKXPNT1KMMAFA6KYCXEZJ1

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

2-001, 2-002, 2-003, 2-005, 2-006, 2-007, 2-008, 2-009, 2-010, 2-011, 2-015, 2-01659069357990552