Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

PROCEDURE PACK - NASAL CANNULA FOR… — 6 UDI-DI variants, MDR

MD Atlas
GINEVRI srl

Data from EUDAMED, last updated May 30, 2026

PROCEDURE PACK - NASAL CANNULA FOR NON-INVASIVE THERAPY

80538473641SN

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: GINEVRI srl

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 80538473641SN
Device name: —
Device model: PROCEDURE PACK - NASAL CANNULA FOR NON-INVASIVE THERAPY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 31, 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

6 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KN254H4G49AVQ0CTHDVZXGY3

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

SMART CANNULA L WITH BONNET 35CM08053847360648
SMART CANNULA L WITH BONNET 40cm08053847360594
SMART CANNULA M WITH BONNET 30cm08053847360587
SMART CANNULA S WITH BONNET 27cm08053847360570
SMART CANNULA XS WITH BONNET 22CM08053847360808
SMART CANNULA XS WITH BONNET 24cm08053847360563