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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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exciplex — 3 UDI-DI variants, MDR (CLARTEIS SAS)

MD Atlas
CLARTEIS SAS

Data from EUDAMED, last updated May 19, 2026

exciplex

376031346EIPL-100DB

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: CLARTEIS SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 376031346EIPL-100DB
Device name: exciplex
Device model: EIPL-100
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: CLARTEIS SAS
SRN: FR-MF-000002542
Country: France
Email: contact@clarteis.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRXFGWCCW68NWKVW4QK80D5P

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

EIPL-PRD-K01-803760313460096
EIPL-PRD-K01-803760313460041
EIPL-PRD-K01-803760313460072