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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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Bolus gel — 4 UDI-DI variants, MDR (LIEVENS-LANCKMAN BV)

MD Atlas
LIEVENS-LANCKMAN BV

Data from EUDAMED, last updated May 23, 2026

Bolus gel

5430003778Bolus30x30TA

4 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: LIEVENS-LANCKMAN BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5430003778Bolus30x30TA
Device name: Bolus gel
Device model: Bolus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: LIEVENS-LANCKMAN BV
SRN: BE-MF-000001979
Country: Belgium
Email: lievens@skynet.be

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KHVJ11AXA311V9H6DNE6V4G3

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

Bolus Gel, 30x30x0,5cm05430003778111
Bolus Gel, 30x30x0,5cm05430003778210
Bolus Gel, 30x30x1,0cm05430003778227
Bolus Gel, 30x30x1cm05430003778203