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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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Schaber , Küretten - Curettes — 6 UDI-DI variants, MDR

MD Atlas
Scholz Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Schaber , Küretten - Curettes

426052621SIFK013K

6 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: Scholz Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426052621SIFK013K
Device name: Schaber , Küretten - Curettes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 2, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KGF6CAMME3XQ0A0M7CGFVFGV

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

Double Curette, 210 mm14260526217501
Fox Curette, 145 mm14260526217532
TAFK803314260526215651
Jansen Double Curette, 160 mm14260526217525
Sharp double curette, combination big, 170 mm14260526217648
Volkmann Double Curette, 160 mm14260526217518