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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

05.0085l — Class I MDR by SCHÖLLY FIBEROPTIC GMBH

MD Atlas
SCHÖLLY FIBEROPTIC GMBH

EUDAMED last updated this device on Feb 25, 2026

05.0085l

42504801FOLIGHTGUIDESHV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SCHÖLLY FIBEROPTIC GMBH
UDI-DI code: 04250480101841
Reference / catalog number: 05.0085l

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Manufacturer information

Organization name: SCHÖLLY FIBEROPTIC GMBH
SRN: DE-MF-000005618
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

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Türkiye		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04250480101841
Basic UDI-DI: 42504801FOLIGHTGUIDESHV
Reference / catalog number: 05.0085l
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: —
Additional information URL: https://www.schoelly.de/en/instructions-for-use-1
Clinical sizes: 3000 MU50
3.5 MU50

EMDN nomenclature code(s)

Z12020480INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES - 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

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Software identification