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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

BOUCHON LLFE V1 PS — Class IIa MDD by HEMODIA SAS

MD Atlas
HEMODIA SAS

EUDAMED last updated this device on Jun 13, 2025

BOUCHON LLFE V1 PS

B-03661379264065

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: HEMODIA SAS
UDI-DI code: 03661379264065
Reference / catalog number: 103297

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Manufacturer information

Organization name: HEMODIA SAS
SRN: FR-MF-000007191
Manufacturer status: Active

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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.

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: BOUCHON LLFE V1 PS
UDI-DI code: 03661379264065
Basic UDI-DI: B-03661379264065
Reference / catalog number: 103297
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Les bouchons Luer Lock fabriqués par Hemodia sont destinés à être utilisés pour l'obturation ou la protection d'autres dispositifs médicaux ayant un embout Luer Lock : seringues, tubulures, cathéters… Ils permettent de garder le dispositif propre et de limiter l'exposition aux germes potentiels.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A070599CAPS OR OBTURATORS - 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

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Software identification