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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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Organization name
UDI-DI code
Reference / catalog number

Scanboby Peek direct implant CC — Class I MDR by AoN Implants

MD Atlas
AoN Implants

EUDAMED last updated this device on May 27, 2026

Scanboby Peek direct implant CC

805626973SPKRD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AoN Implants
UDI-DI code: 08053632626119
Reference / catalog number: ASB0000000PPC

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View device family (Basic UDI)

Manufacturer information

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

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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.

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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: Scanboby Peek direct implant CC
UDI-DI code: 08053632626119
Basic UDI-DI: 805626973SPKRD
Reference / catalog number: ASB0000000PPC
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: Scanboby Peek direct implant CC
Additional information URL: https://aonimplants.it/IFU/
Clinical sizes: CC

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08053632626119

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UDI-PI DataMatrix

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

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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

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