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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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Spekulum - Specula — 2 UDI-DI variants, MDR (Scholz Medical GmbH)

MD Atlas
Scholz Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Spekulum - Specula

426052621SIOK015J

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Scholz Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426052621SIOK015J
Device name: Spekulum - Specula
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Scholz Medical GmbH
SRN: DE-MF-000008955
Country: Germany
Email: info@scholz-medical.de
Phone: +49 8062 8070801

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

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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

Kilian Nose Speculum, 70 mm shaft, 120 mm14260526217211
Kilian Speculum, 30 mm shaft, 120 mm14260526217242