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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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Demo Zygo AoN Implants — 28 UDI-DI variants, MDR (AoN Implants)

MD Atlas
AoN Implants

Data from EUDAMED, last updated May 31, 2026

Demo Zygo AoN Implants

805626973DZYQU

28 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: AoN Implants

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Device characteristics

Reusable

Legacy certificates

Certificate number: 0425-MDR-030062-01
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ICIM S.P.A. (0425)
Validity: Oct 3, 2024 → Jan 16, 2029

Identity & classification

Basic UDI-DI: 805626973DZYQU
Device name: Demo Zygo AoN Implants
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: AoN Implants
SRN: IT-MF-000011061
Country: Italy
Email: info@aonimplants.com
Phone: +390444614994

Variants by status

UDI-DI variants

28 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR3CYHXFGT6KVMH43V91G5SZ

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

Trial Zygo D.4.00 L.6008056269736602
Trial Zygo D.4.00 L.2808056269736473
ATI3528000ZYC08056269736336

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