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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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EPTE BIPOLAR — 2 UDI-DI variants, MDR (IONCLINICS & DEIONIC, S.L.)

MD Atlas
IONCLINICS & DEIONIC, S.L.

Data from EUDAMED, last updated May 23, 2026

EPTE BIPOLAR

8437023158EPTEV02LQ

2 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: IONCLINICS & DEIONIC, S.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8437023158EPTEV02LQ
Device name: EPTE BIPOLAR
Device model: EPTEV02
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 27, 2023

Manufacturer & authorised representative

Manufacturer

Name: IONCLINICS & DEIONIC, S.L.
SRN: ES-MF-000020207
Country: Spain
Email: info@ionclinics.com
Phone: +34 960606200

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H6BRFKBSKP8C6ERRTSW9C9R9

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

EPTEV02DEV0108437023158012
EPTEV02DEV0208437023158029