Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Phyxiom Clinical Decision Support… — 1 UDI-DI variant, MDR

MD Atlas
Phyxiom Limited

Data from EUDAMED, last updated May 31, 2026

Phyxiom Clinical Decision Support Software

539155293PHYX-CDS-00252

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Phyxiom Limited

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 539155293PHYX-CDS-00252
Device name: Phyxiom Clinical Decision Support Software
Device model: PHYX-CDS-002
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: May 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Phyxiom Limited
SRN: IE-MF-000054005
Country: Ireland
Email: info@phyxiom.com
Phone: +353-18328649

Variants by status

UDI-DI variants

1 UDI-DI variant

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KSFXBVPKKFYJXY3HYQJ9C9A9

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

Phyxiom53915529300024