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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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MEDICAL FISYO GUANCIALE — 6 UDI-DI variants, MDR

MD Atlas
IL MATERASSIFICIO S.R.L.

Data from EUDAMED, last updated May 31, 2026

MEDICAL FISYO GUANCIALE

805071446MEDICALFISYOEP

6 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: IL MATERASSIFICIO S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805071446MEDICALFISYOEP
Device name: MEDICAL FISYO GUANCIALE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: IL MATERASSIFICIO S.R.L.
SRN: IT-MF-000051614
Country: Italy
Email: amministrazione@ilmaterassificio.it
Phone: +39 042434170

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KFK3C2X4G7CRNS6TEN927NGE

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

MEDICAL FISYO GUANCIALE H1408050714460043
MEDICAL FISYO GUANCIALE H608050714460005
MEDICAL FISYO GUANCIALE H 1608050714460050
MEDICAL FISYO GUANCIALE H1008050714460029
MEDICAL FISYO GUANCIALE H808050714460012
MEDICAL FISYO GUANCIALE H1208050714460036