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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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SYNC FLOW CANNULA M — 1 UDI-DI variant, MDD (GINEVRI srl)

MD Atlas
GINEVRI srl

Data from EUDAMED, last updated May 31, 2026

SYNC FLOW CANNULA M

B-08053847362802

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: GINEVRI srl

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: IT256902
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: BUREAU VERITAS ITALIA S.P.A. (1370)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08053847362802
Device name: SYNC FLOW CANNULA M
Device model: SYNC FLOW CANNULA M
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Feb 11, 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

1 UDI-DI variant

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basicUdiUlid01KH68TBSYV1CCMXH6JMTWGRFA

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

SYNC FLOW CANNULA M08053847362802