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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

Veye Clinic — Class I MDR by Aidence B.V.

MD Atlas
Aidence B.V.

EUDAMED last updated this device on Jul 4, 2023

Veye Clinic

++B865VeyeClinicLJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aidence B.V.
UDI-DI code: B865VEYECLINIC0104X0
Reference / catalog number: 1

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View device family (Basic UDI)

Manufacturer information

Organization name: Aidence B.V.
SRN: NL-MF-000000534
Manufacturer status: Active

Related devices

Veye Clinic++B865VeyeClinicLJOn the market Veye Clinic++B865VeyeClinicLJOn the market Veye Clinic++B865VeyeClinicLJOn the market Veye Clinic++B865VeyeClinicLJOn the market Veye Clinic++B865VeyeClinicLJOn the market

Certificates

Certificate health across this manufacturer's portfolio.

SCAR-15.2.1.1Amended
Quality management systemNotified body: 3022Expiry: Oct 1, 2030
2245855CE01Issued
Quality management systemNotified body: 0344Expiry: Oct 1, 2025

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

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

Device identification

Trade name: Veye Clinic
UDI-DI code: B865VEYECLINIC0104X0
Basic UDI-DI: ++B865VeyeClinicLJ
Reference / catalog number: 1
Issuing entity: HIBCC

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: Veye Clinic is intended to support qualified medical professionals in patient follow-up management.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

Z11069082VARIOUS DIGITAL BIOIMAGING MANAGEMENT INSTRUMENTS - SOFTWARE 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

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