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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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Viofor JPS System Delux — 1 UDI-DI variant, MDD

MD Atlas
Med & Life Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Viofor JPS System Delux

B-05905155200020

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Med & Life Sp. z o.o.

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Device characteristics

Active device

Legacy certificates

Certificate number: TNP/MDD/0300/4086/2020
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TUV NORD Polska Sp. z o.o (2274)
Validity: Jan 10, 2023

Identity & classification

Basic UDI-DI: B-05905155200020
Device name: Viofor JPS System Delux
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Med & Life Sp. z o.o.
SRN: PL-MF-000024639
Country: Poland
Email: biuro@medandlife.com
Phone: +22 759 15 15

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSJFC2VRGP2AAW9XZTHD4MNS

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

Viofor JPS System Delux05905155200020