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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

SLC D. 4.2 L. 11.5 OsTiOX CC — Class IIb MDR by AoN Implants

MD Atlas
AoN Implants

EUDAMED last updated this device on May 11, 2026

SLC D. 4.2 L. 11.5 OsTiOX CC

805626973IMPPU

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AoN Implants
UDI-DI code: 08056269735094
Reference / catalog number: ALC42115N200C

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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: SLC D. 4.2 L. 11.5 OsTiOX CC
UDI-DI code: 08056269735094
Basic UDI-DI: 805626973IMPPU
Reference / catalog number: ALC42115N200C
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://aonimplants.it/IFU/
Clinical sizes: 4.2 MU50
11.5 MU50
CC
Octa

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08056269735094

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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.

P01020101DENTAL IMPLANTS

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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