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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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ET-NFC-G1 — 1 UDI-DI variant, MDD (ADVANCED ELECTRONIC BIOSYSTEM SRL)

MD Atlas
ADVANCED ELECTRONIC BIOSYSTEM SRL

Data from EUDAMED, last updated May 31, 2026

ET-NFC-G1

B-08056214670029

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: ADVANCED ELECTRONIC BIOSYSTEM SRL

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: 0068/QCO-DM/382-2021
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: MTIC InterCert S.r.l. (0068)
Validity: May 27, 2024

Identity & classification

Basic UDI-DI: B-08056214670029
Device name: ET-NFC-G1
Device model: ET-NFC-G1
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: ADVANCED ELECTRONIC BIOSYSTEM SRL
SRN: IT-MF-000041046
Country: Italy
Email: p.marini@aebiosystem.com
Phone: +39 3932018615

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KRGWZGRP2EXC2T26RS1PWV0Z

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

ET-NFC-G108056214670029