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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

BPPC18140700040 — Class IIa MDR by Life Vascular Devices…

MD Atlas
Life Vascular Devices Biotech, S.L.

EUDAMED last updated this device on May 22, 2026

BPPC18140700040

84353873oceanus186A

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Life Vascular Devices Biotech, S.L.
UDI-DI code: 08435387307084
Reference / catalog number: BPPC18140700040

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Manufacturer information

Organization name: Life Vascular Devices Biotech, S.L.
SRN: ES-MF-000019783
Manufacturer status: Active

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Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Mar 24, 2015	May 22, 2026

Device identification

Trade name: not provided
UDI-DI code: 08435387307084
Basic UDI-DI: 84353873oceanus186A
Reference / catalog number: BPPC18140700040
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: ATP balloon dilatation catheter (for 0,018" guidewire)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

C010402020101PTA BALLOON DILATATION 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

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.