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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 18 — 153 UDI-DI variants, MDR

MD Atlas
Life Vascular Devices Biotech, S.L.

Data from EUDAMED, last updated May 23, 2026

iVascular oceanus 18

84353873oceanus186A

153 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: 84353873oceanus186A
Device name: iVascular oceanus 18
Device model: oceanus 18
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 13, 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

153 UDI-DI variants

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Applied filters

basicUdiUlid01KRGDF39BWW08807GBDFAYS9G

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

No registered UDI-DI variants for this device family.