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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

EUROLIGHT E25, HL, ophthalmoscope… — Class I MDR

MD Atlas
Kirchner & Wilhelm GmbH + Co KG

EUDAMED last updated this device on Oct 28, 2022

EUROLIGHT E25, HL, ophthalmoscope head, only, black

4030155KaWe0102YT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kirchner & Wilhelm GmbH + Co KG
UDI-DI code: 04030155017628
Reference / catalog number: 01.85255.021

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Manufacturer information

Organization name: Kirchner & Wilhelm GmbH + Co KG
SRN: DE-MF-000006338
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW147
EUDAMED did not publish a description for this code.
CW258
An error may cause extensive heat posing a threat of burn injury. If the devices heats excessively, immediately turn the handle off.

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: EUROLIGHT E25, HL, ophthalmoscope head, only, black
UDI-DI code: 04030155017628
Basic UDI-DI: 4030155KaWe0102YT
Reference / catalog number: 01.85255.021
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: Diagnostic instrument for optical examination of the fundus of the eye by direct ophthalmoscopy.
Additional information URL: https://www.kawemed.com/download/gebrauchsanweisungen/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12120114OPHTHALMOSCOPES

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

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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.