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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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DUAL BORE CANNULAE / CANNULA DUAL BORE — 6 UDI-DI variants, MDR

MD Atlas
AKTIVE SRL

Data from EUDAMED, last updated May 30, 2026

DUAL BORE CANNULAE / CANNULA DUAL BORE

8052276FT0001ID8CN

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: AKTIVE SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8052276FT0001ID8CN
Device name: DUAL BORE CANNULAE / CANNULA DUAL BORE
Device model: DUAL BORE CANNULAE / CANNULA DUAL BORE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 30, 2022

Manufacturer & authorised representative

Manufacturer

Name: AKTIVE SRL
SRN: IT-MF-000007813
Country: Italy
Email: quality@aktive-corp.com
Phone: 06.88640509

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GK43GADRMY8W40G84N149427

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

Cannula Dual Bore 23G08052276027283
Dual Bore Cannula 20G08052276027276
Dual Bore Cannula 23G, 36mm08052276027290
Dual Bore Cannula 25G08052276027306
Dual Bore Cannula 25G, 36mm08052276027313
Dual Bore Cannula 27G08052276027450