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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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LCEV — 3 UDI-DI variants, MDR (LEVO AG)

MD Atlas
LEVO AG

Data from EUDAMED, last updated May 23, 2026

LCEV

7613045_LCEV_3B

3 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: LEVO AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7613045_LCEV_3B
Device name: LCEV
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: LEVO AG
SRN: CH-MF-000008751
Country: Switzerland
Email: office@levo.ch
Phone: +41566184411

Authorised representative

Name: be-on-market GmbH
SRN: DE-AR-000006148
Country: Germany

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K2Y5R97T6E739RV8JHYF32GX

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

JR/XS/35/4007613045034331
LCEV/L-XL/42/5107613045038841
KID/XS/35/3307613045034256