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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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Arthroscopes — 16 UDI-DI variants, MDR (SCHÖLLY FIBEROPTIC GMBH)

MD Atlas
SCHÖLLY FIBEROPTIC GMBH

Data from EUDAMED, last updated May 23, 2026

Arthroscopes

42504801ARTHROSCOPESSU

16 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: SCHÖLLY FIBEROPTIC GMBH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42504801ARTHROSCOPESSU
Device name: —
Device model: Arthroscopes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: SCHÖLLY FIBEROPTIC GMBH
SRN: DE-MF-000005618
Country: Germany
Email: info@schoelly.de
Phone: 076669080

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K108G72M9DRNRPE6BNF2WFRZ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

21.0011a04250480102091
21.0003a04250480101476
21.0008a04250480102084
21.0621a04250480101926
21.0101a04250480102107
21.0619a04250480102114
21.0008a04250480101490
21.0101a04250480101131
21.0617a04250480109304
21.0003a04250480102077
21.0011a04250480101520
21.0621a04250480102121
21.0101a04250480101636
21.0619a04250480101896
21.0008a04250480101827
21.0617a04250480101872