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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

NOVA.light — Class I MDR by NEXOR MEDICAL GmbH

MD Atlas
NEXOR MEDICAL GmbH

EUDAMED last updated this device on Jan 14, 2025

NOVA.light

426075377000Z12010701B5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NEXOR MEDICAL GmbH
UDI-DI code: 04260753770513
Reference / catalog number: 06-000-600

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Manufacturer information

Organization name: NEXOR MEDICAL GmbH
SRN: DE-MF-000005527
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: NOVA.light
UDI-DI code: 04260753770513
Basic UDI-DI: 426075377000Z12010701B5
Reference / catalog number: 06-000-600
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: surgical light head to be combined to a surgical light set
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12010780SCIALYTIC LAMP LIGHTING SYSTEMS - HARDWARE 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

This device is not currently linked to any other device.

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.