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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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Stone Retrieval Device — 59 UDI-DI variants, MDR

MD Atlas
EPflex Feinwerktechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Stone Retrieval Device

42556056srd7T

59 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: EPflex Feinwerktechnik GmbH

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 1000265993
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Oct 27, 2025 → Nov 8, 2028

Identity & classification

Basic UDI-DI: 42556056srd7T
Device name: Stone Retrieval Device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: EPflex Feinwerktechnik GmbH
SRN: DE-MF-000005425
Country: Germany
Email: ben.olwal@epflex.com

Variants by status

UDI-DI variants

59 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JCJJ6AFMMTP54ADSDEYMYTZQ

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

4000944504255605604863
4101023404255605605006
4001313504255605606041
4701225304255605605501
4000961204255605604924
4201083804255605605167
4101024004255605605044
4900810904255605605846
4801249304255605606225

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