Pricing Sign in

Role
Country
Date of registration
Address

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.

Organization name
UDI-DI code
Reference / catalog number

Scanbody Universal Peek — Class I MDR by AoN Implants

MD Atlas
AoN Implants

EUDAMED last updated this device on May 27, 2026

Scanbody Universal Peek

805626973SPKRD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AoN Implants
UDI-DI code: 08053632626126
Reference / catalog number: ASB00000SUPP0

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?

View device family (Basic UDI)

Manufacturer information

Organization name: AoN Implants
SRN: IT-MF-000011061
Manufacturer status: Active

Related devices

Extra-Long Manual Prosthetic Wrench 1.20 EH805626973CVMPKOn the market 2G h.10 mm ridge preparer805626973PREQQOn the market 2G h.11,5 mm ridge preparer805626973PREQQOn the market 2G h.13 mm ridge preparer805626973PREQQOn the market 2G h.15 mm ridge preparer805626973PREQQOn the market

Certificates

Certificate health across this manufacturer's portfolio.

0425-MDR-030062-01Issued
Quality management systemNotified body: 0425Expiry: Jan 16, 2029

Critical warnings

No critical warnings reported for this device.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement	Jan 1, 2009	Still on market
Spain	Jan 1, 2025	Still on market

Device identification

Trade name: Scanbody Universal Peek
UDI-DI code: 08053632626126
Basic UDI-DI: 805626973SPKRD
Reference / catalog number: ASB00000SUPP0
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Scanbody Universal Peek
Additional information URL: https://aonimplants.it/IFU/
Clinical sizes: Universale

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08053632626126

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

L159099ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas