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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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BONNET for NIV — 3 UDI-DI variants, MDR (GINEVRI srl)

MD Atlas
GINEVRI srl

Data from EUDAMED, last updated May 31, 2026

BONNET for NIV

80538473637SX

3 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: GINEVRI srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80538473637SX
Device name: BONNET for NIV
Device model: BONNET for NIV - SMALL SIZES KIT (2XXS, 2XS, 2S)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: GINEVRI srl
SRN: IT-MF-000034527
Country: Italy
Email: mail@ginevri.com
Phone: +39 069345100

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KKXNN35DDAVEPD5RTZHAHMQF

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

BONNET for NIV - LARGE SIZES KIT (2M, 2L, 2XL)08053847360853
BONNET for NIV - MEDIUM SIZES KIT (2S, 2M, 2L)08053847360846
BONNET for NIV - SMALL SIZES KIT (2XXS, 2XS, 2S)08053847360839