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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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Organization name
UDI-DI code
Reference / catalog number

Bolus Gel, 30x30x1,0cm — Class I MDR by LIEVENS-LANCKMAN BV

MD Atlas
LIEVENS-LANCKMAN BV

EUDAMED last updated this device on Feb 19, 2026

Bolus Gel, 30x30x1,0cm

5430003778Bolus30x30TA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LIEVENS-LANCKMAN BV
UDI-DI code: 05430003778227
Reference / catalog number: BL-9910 - 3 pces

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Manufacturer information

Organization name: LIEVENS-LANCKMAN BV
SRN: BE-MF-000001979
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW261
Do not apply to broken skin

Market distribution

Primary placement in Belgium; available across 1 country total.

Placed on the market in Belgium; per-country availability dates not published.

Device identification

Trade name: Bolus Gel, 30x30x1,0cm
UDI-DI code: 05430003778227
Basic UDI-DI: 5430003778Bolus30x30TA
Reference / catalog number: BL-9910 - 3 pces
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: -
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 30x30x1 cm

EMDN nomenclature code(s)

T030499RADIOTHERAPY PROTECTION DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.