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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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Euroampli Alien Cardio - Vers. 2121 — 1 UDI-DI variant, MDD

MD Atlas
eurocolumbus s.r.l.

Data from EUDAMED, last updated May 31, 2026

Euroampli Alien Cardio - Vers. 2121

B-08055715530122

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: eurocolumbus s.r.l.

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Device characteristics

Active device

Legacy certificates

Certificate number: 160/MDD
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: IMQ ISTITUTO ITALIANO DEL MARCHIO DI QUALITÀ S.P.A. (0051)
Validity: Jan 8, 2024

Identity & classification

Basic UDI-DI: B-08055715530122
Device name: Euroampli Alien Cardio - Vers. 2121
Device model: Euroampli Alien Cardio
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Oct 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: eurocolumbus s.r.l.
SRN: IT-MF-000016861
Country: Italy
Email: eurocol@eurocol.it
Phone: +39 02 89122273

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01K6F58HB7BSGPFANCGTQT5J1V

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

Euroampli Alien Cardio - Vers. 212108055715530122