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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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Multi-Snare® — 7 UDI-DI variants, MDR (PFM medical mepro GmbH)

MD Atlas
PFM medical mepro GmbH

Data from EUDAMED, last updated May 23, 2026

Multi-Snare®

4042301C0190AAJ7

7 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: PFM medical mepro GmbH

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 4042301C0190AAJ7
Device name: Multi-Snare®
Device model: Snare
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: PFM medical mepro GmbH
SRN: DE-MF-000005190
Country: Germany
Email: mepro-info@pfmmedical.com
Phone: +496873 9011-0

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KRNKJRSRRW3QWR6NSJRXM605

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

Multi-Snare®04042301033604
Multi-Snare®04042301074409
Multi-Snare®04042301061829
Multi-Snare®04042301061805
Multi-Snare®04042301033581
Multi-Snare®04042301061812
Multi-Snare®04042301033567