Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Mucotomi AoN Implants — 6 UDI-DI variants, MDR (AoN Implants)

MD Atlas
AoN Implants

Data from EUDAMED, last updated May 31, 2026

Mucotomi AoN Implants

805626973MUCQE

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: AoN Implants

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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: 805626973MUCQE
Device name: Mucotomi 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

6 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KR3F32BJN5AK0J4YY7PKQ70T

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

AUN41000MU00008056269738330
Mucotomy 2G Ø 4.70 L.24mm08056269738385
Mucotomy 2G Ø 4.70 L.29mm08056269738378
Mucotomy B408056269738354
Mucotomy B508056269738361
Universal mucotomy Ø5mm08056269738347