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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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SEDIE DA COMODO — 2 UDI-DI variants, MDR (PRAXIS MEDICAL NETWORK SRL)

MD Atlas
PRAXIS MEDICAL NETWORK SRL

Data from EUDAMED, last updated May 30, 2026

SEDIE DA COMODO

80584817602206Z

2 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: PRAXIS MEDICAL NETWORK SRL

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Device characteristics

No device characteristics flagged

Clinical investigations

Investigation number: UN-CE-05-J
Registered: No
Countries: China

Identity & classification

Basic UDI-DI: 80584817602206Z
Device name: SEDIE DA COMODO
Device model: SEDIE DA COMODO PMN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 17, 2021

Manufacturer & authorised representative

Manufacturer

Name: PRAXIS MEDICAL NETWORK SRL
SRN: IT-MF-000017626
Country: Italy
Email: info@praxismedicalnetwork.com
Phone: +39 06 3751 5696

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FQ41Y7220N85GGBKS1QB7Q0C

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

PX1625108058481765095
PX1625008058481761219