Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

BPPC14N20025004008435387317885
BPPC14N10030015008435387308142
BPPC14N10015002008435387310886
BPPC14N20015004008435387317762
BPPC14N15020015008435387308333
BPPC14N10040012008435387308258
BPPC14N20040006008435387318073
BPPC14N10035008008435387308180
BPPC14N20012501008435387317700
BPPC14N17030012008435387317571
BPPC14N10020012008435387308012
BPPC14N15025012008435387308388
BPPC14N15015001008435387310954
BPPC14N170300040 08435387317540
BPPC14N15015001508435387310961
BPPC14N17035004008435387317601
BPPC14N17025008008435387317502
BPPC14N10025015008435387308081
BPPC14N20030015008435387317984
BPPC14N17012502008435387317328
BPPC14N17015001008435387317335
BPPC14N20035004008435387318004
BPPC14N10025006008435387308050
BPPC14N17015001508435387317342
BPPC14N15035004008435387308470

1 2 3 4 5