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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

Bonelogic CMF Orbital — Class I MDD by Disior Oy

MD Atlas
Disior Oy

EUDAMED last updated this device on Dec 12, 2025

Bonelogic CMF Orbital

B-Bonelogic_CMFOrbital_WP

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Disior Oy
UDI-DI code: D-Bonelogic_CMFOrbital_WP
Reference / catalog number: Bonelogic CMF Orbital

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Manufacturer information

Organization name: Disior Oy
SRN: FI-MF-000002448
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

Placed on the market in Finland; per-country availability dates not published.

Device identification

Trade name: Bonelogic CMF Orbital
UDI-DI code: D-Bonelogic_CMFOrbital_WP
Basic UDI-DI: B-Bonelogic_CMFOrbital_WP
Reference / catalog number: Bonelogic CMF Orbital
Issuing entity: EUDAMED

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://smart.paragon28.com/disior-ltd/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z110603PICTURE ARCHIVING AND COMMUNICATION SYSTEMS

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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

FI20/00000020Issued
Quality management systemNotified body: 0598Expiry: May 30, 2026