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™07630033300551
Europa Ultra™07630033300926
Europa Ultra™07630033300186
Europa Ultra™07630033300490
Europa Ultra™07630033300704
Europa Ultra™07630033300445
Europa Ultra™07630033301053
Europa Ultra™07630033300391
Europa Ultra™07630033300636
Europa Ultra™07630033300544
Europa Ultra™07630033300339
Europa Ultra™07630033300797
Europa Ultra™07630033300483
Europa Ultra™07630033300865
Europa Ultra™07630033301046
Europa Ultra™07630033300827
Europa Ultra™07630033300889
Europa Ultra™07630033300513
Europa Ultra™07630033300728
Europa Ultra™07630033300995
Europa Ultra™07630033300155
Europa Ultra™07630033300018
Europa Ultra™07630033300094
Europa Ultra™07630033300179
Europa Ultra™07630033300957

1 2 3 4 5