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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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CUSCINO FIBRA CAVA — 6 UDI-DI variants, MDR

MD Atlas
tecnologia ospedaliera srl

Data from EUDAMED, last updated May 30, 2026

CUSCINO FIBRA CAVA

805076271600BU

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: tecnologia ospedaliera srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805076271600BU
Device name: CUSCINO FIBRA CAVA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: tecnologia ospedaliera srl
SRN: IT-MF-000033201
Country: Italy
Email: anna.sevignani@tecnologiaospedaliera.com
Phone: 0458510744

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JF7FCZVHPJEC0DHGXZ0E0JZM

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

HP600608050762712903
HP600508050762712897
HP600308050762712729
HP600108050762712705
HP600208050762712712
HP600008050762712736