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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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PiCSO Impulse Power Cord — 5 UDI-DI variants, MDR (Miracor Medical SA)

MD Atlas
Miracor Medical SA

Data from EUDAMED, last updated May 23, 2026

PiCSO Impulse Power Cord

05430002982103000XPH

5 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: Miracor Medical SA

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 05430002982103000XPH
Device name: PiCSO Impulse Power Cord
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 14, 2022

Manufacturer & authorised representative

Manufacturer

Name: Miracor Medical SA
SRN: BE-MF-000001089
Country: Belgium
Email: vderudder@miracormedical.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FY48N2KCE68BE7886SP6VKHE

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

PiCSO Impulse Power Cord, CH05430002982069
PiCSO Impulse Power Cord, EU05430002982045
PiCSO Impulse Power Cord, IT05430002982076
PiCSO Impulse Power Cord, UK05430002982052
PiCSO Impulse Power Cord, US/CAN05430002982083