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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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Single-Use Patient Part (SUPP) — 1 UDI-DI variant, MDR

MD Atlas
Vimex Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Single-Use Patient Part (SUPP)

5907595122PV-5201SUPPAP

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Vimex Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5907595122PV-5201SUPPAP
Device name: Single-Use Patient Part (SUPP)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Vimex Sp. z o.o.
SRN: PL-MF-000008668
Country: Poland
Email: office@vimex.eu
Phone: +48322308682

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KSPZG4DHEX07BJPEYYZV1320

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

5201-6105907595122474