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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

31.0810a — Class IIa MDR by SCHÖLLY FIBEROPTIC GMBH

MD Atlas
SCHÖLLY FIBEROPTIC GMBH

EUDAMED last updated this device on Apr 1, 2026

31.0810a

42504801SINUSCOPESAL

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SCHÖLLY FIBEROPTIC GMBH
UDI-DI code: 04250480102169
Reference / catalog number: 31.0810a

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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: 04250480102169
Basic UDI-DI: 42504801SINUSCOPESAL
Reference / catalog number: 31.0810a
Issuing entity: GS1

Classification

Risk category: Class IIa
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: 0 MU105
Working length — 187 MU50
Outer diameter of insertion portion — 2.7 MU50

EMDN nomenclature code(s)

Z12021008RHINOSCOPES

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
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Software identification