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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

Bone Level Temporary Abutment… — Class IIb MDD by Novodent SA

MD Atlas
Novodent SA

EUDAMED last updated this device on Jul 31, 2025

Bone Level Temporary Abutment Non-Hex

B-07640168181574

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Novodent SA
UDI-DI code: 07640168181574
Reference / catalog number: S-BTAN65

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Manufacturer information

Organization name: Novodent SA
SRN: CH-MF-000023309
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Türkiye; available across 2 countries total.

Country	On market since	Until
TürkiyePrimary placement	Jan 29, 2021	Still on market
Sweden	Jul 1, 2019	Still on market

Device identification

Trade name: Bone Level Temporary Abutment Non-Hex
UDI-DI code: 07640168181574
Basic UDI-DI: B-07640168181574
Reference / catalog number: S-BTAN65
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Bone Level Temporary Abutment Non-Hex
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P01020180DENTAL IMPLANTS - ACCESSORIES

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

UDI-PI traceability

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Software identification