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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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Hypo-/ hyperthermia systems — 4 UDI-DI variants, MDR

MD Atlas
pfm medical hico GmbH

Data from EUDAMED, last updated May 23, 2026

Hypo-/ hyperthermia systems

4042301Z1204ACVX

4 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: pfm medical hico GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4042301Z1204ACVX
Device name: Hypo-/ hyperthermia systems
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: pfm medical hico GmbH
SRN: DE-MF-000012921
Country: Germany
Email: hico@pfmmedical.com
Phone: +49221 37678-0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JT893JFNJX1SK2HCNGX7CCAS

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

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