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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

LomiFlow — Class III MDD by L2MTech GmbH

MD Atlas
L2MTech GmbH

EUDAMED last updated this device on Jul 22, 2023

LomiFlow

B-04262375060003

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: L2MTech GmbH
UDI-DI code: 04262375060003
Reference / catalog number: LF25010

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Manufacturer information

Organization name: L2MTech GmbH
SRN: DE-MF-000036711
Manufacturer status: Active

Critical warnings

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

CW001
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Belgium		Still on market

Device identification

Trade name: LomiFlow
UDI-DI code: 04262375060003
Basic UDI-DI: B-04262375060003
Reference / catalog number: LF25010
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC 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: 10 MU50

EMDN nomenclature code(s)

C010401020101PTCA BALLOON DILATION CATHETERS

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

L2M-MKT-LMTB-04262473120210On the market

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.