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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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KOPFRAUMFRÄSER CS 3,5 — 14 UDI-DI variants, MDR

MD Atlas
Meditec Source GmbH & Co. KG

Data from EUDAMED, last updated Jun 2, 2026

KOPFRAUMFRÄSER CS 3,5

426246385PG249T

14 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: Meditec Source GmbH & Co. KG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 426246385PG249T
Device name: KOPFRAUMFRÄSER CS 3,5
Device model: Fräser
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: Meditec Source GmbH & Co. KG
SRN: DE-MF-000006490
Country: Germany
Email: martin.streng@meditec-source.com
Phone: 017610429389

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KT1KPK3PZF5J09CKBNHGH1NV

Format

Summary

30 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
Market country
Issuing entity
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

2420-11104262463851247
2420-11004262463851230
2420-11204262463852091
2420-22204262463851261
2420-22104262463851254
2420-12104262463850028
2420-12204262463850035
2420-31104262463851278
2420-31204262463851285
2420-35204262463851308
2420-35104262463851292
2420-40104262463851315
2420-50104262463851322
2420-60104262463851339