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.

Europa Ultra Coronary Balloon Catheter — 110 UDI-DI variants, MDR

MD Atlas
Rontis Corporation SA

Data from EUDAMED, last updated May 23, 2026

Europa Ultra Coronary Balloon Catheter

076300333EF_CBLCATHGG

110 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: Rontis Corporation SA

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

Legacy certificates

Certificate number: 44912221174
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: TÜV NORD CERT GmbH (0044)
Validity: Mar 15, 2024 → Mar 14, 2029

Identity & classification

Basic UDI-DI: 076300333EF_CBLCATHGG
Device name: Europa Ultra Coronary Balloon Catheter
Device model: Europa Ultra™ Family
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Apr 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: Rontis Corporation SA
SRN: CH-MF-000031411
Country: Switzerland
Email: info@rontis.com

Authorised representative

Name: RONTIS HELLAS MEDICAL AND PHARMACEUTICAL PRODUCTS S.A.
SRN: GR-AR-000023077
Country: Greece
Phone: +302106109090

Variants by status

UDI-DI variants

110 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

basicUdiUlid01HTCZ53NH7EFBEV8SEDVHAY0B

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

Europa Ultra™07630033301008
Europa Ultra™07630033300230
Europa Ultra™07630033300599
Europa Ultra™07630033300285
Europa Ultra™07630033300056
Europa Ultra™07630033300032
Europa Ultra™07630033300988
Europa Ultra™07630033300858
Europa Ultra™07630033300568
Europa Ultra™07630033300841
Europa Ultra™07630033300063
Europa Ultra™07630033300384
Europa Ultra™07630033300940
Europa Ultra™07630033300117
Europa Ultra™07630033301084
Europa Ultra™07630033300469
Europa Ultra™07630033300902
Europa Ultra™07630033301015
Europa Ultra™07630033300834
Europa Ultra™07630033300667
Europa Ultra™07630033300650
Europa Ultra™07630033301039
Europa Ultra™07630033300933
Europa Ultra™07630033300261
Europa Ultra™07630033300087

1 2 3 4 5