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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

BPPC18170500150 — Class IIa MDR by Life Vascular Devices…

MD Atlas
Life Vascular Devices Biotech, S.L.

EUDAMED last updated this device on May 29, 2026

BPPC18170500150

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: 08435387318509
Reference / catalog number: BPPC18170500150

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View device family (Basic UDI)

Manufacturer information

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

Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

2023 CR 0011Supplemented
Quality management systemNotified body: 0318Expiry: Dec 21, 2028
G10 103542 0002Issued
Quality management systemNotified body: 0123Expiry: Feb 23, 2028

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Mar 24, 2015	May 29, 2026

Device identification

Trade name: not provided
UDI-DI code: 08435387318509
Basic UDI-DI: 84353873oceanus186A
Reference / catalog number: BPPC18170500150
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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