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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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MATERASSO ZEFIRO — 12 UDI-DI variants, MDR (Dorsal s.r.l)

MD Atlas
Dorsal s.r.l

Data from EUDAMED, last updated May 30, 2026

MATERASSO ZEFIRO

805201108MZEFI4V

12 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: Dorsal s.r.l

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805201108MZEFI4V
Device name: MATERASSO ZEFIRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 31, 2025

Manufacturer & authorised representative

Manufacturer

Name: Dorsal s.r.l
SRN: IT-MF-000048854
Country: Italy
Email: info@dorsal.it
Phone: +39 0438 933003

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01K1D82G40AYT919E1A8HCRZNF

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

MZEFI08052011081716
MZEFI08052011080023
MZEFI08052011080016
MZEFI08052011081822
MZEFI08052011080009
MZEFI08052011080054
MZEFI08052011080047
MZEFI08052011081839
MZEFI08052011080030
MZEFI08052011080061
MZEFI08052011081815
MZEFI08052011081709