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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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Lenke Pfriem gerade — 2 UDI-DI variants, MDR

MD Atlas
Meditec Source GmbH & Co. KG

Data from EUDAMED, last updated May 31, 2026

Lenke Pfriem gerade

426246385PG039K

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: Meditec Source GmbH & Co. KG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 426246385PG039K
Device name: Lenke Pfriem gerade
Device model: 0301-180
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 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

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7HGVXZWVJXVG2CE320EY3Y

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

Feeler04262463852138
Feeler04262463852121