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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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iVascular oceanus 14pro — 157 UDI-DI variants, MDR

MD Atlas
Life Vascular Devices Biotech, S.L.

Data from EUDAMED, last updated May 23, 2026

iVascular oceanus 14pro

84353873oceanus1462

157 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Life Vascular Devices Biotech, S.L.

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 84353873oceanus1462
Device name: iVascular oceanus 14pro
Device model: oceanus 14pro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Life Vascular Devices Biotech, S.L.
SRN: ES-MF-000019783
Country: Spain
Email: regulatory@ivascular.global
Phone: + 34 936724711

Variants by status

UDI-DI variants

157 UDI-DI variants

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Applied filters

basicUdiUlid01KPWS9977WVMHHXKHEF30WS0D

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

BPPC14N17020001508435387317403
BPPC14N10040006008435387308234
BPPC14N10035012008435387308197
BPPC14N10015008008435387307978
BPPC14N20020002008435387317816
BPPC14N10015001508435387310862
BPPC14N20025015008435387317922

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