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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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Impianti Dentali AoN Implants — 617 UDI-DI variants, MDR

MD Atlas
AoN Implants

Data from EUDAMED, last updated May 31, 2026

Impianti Dentali AoN Implants

805626973IMPPU

617 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: AoN Implants

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Device characteristics

Implantable

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: 805626973IMPPU
Device name: Impianti Dentali AoN Implants
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 7, 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

617 UDI-DI variants

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Applied filters

basicUdiUlid01KR1DVMYQCDGNYC2Y7GYYAY5W

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

No registered UDI-DI variants for this device family.