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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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Trift PTA Balloon Dilatation Catheter — 238 UDI-DI variants, MDR

MD Atlas
Cnovate Medical B.V.

Data from EUDAMED, last updated May 31, 2026

Trift PTA Balloon Dilatation Catheter

872062130005AK

238 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: Cnovate Medical B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 872062130005AK
Device name: Trift PTA Balloon Dilatation Catheter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: Cnovate Medical B.V.
SRN: NL-MF-000006042
Country: Netherlands
Email: cs@cnovate.eu

Variants by status

UDI-DI variants

238 UDI-DI variants

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Applied filters

basicUdiUlid01JT2734NP6NSPQ6SP47T4ARCW

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

Trift08720621347347
Trift08720621348283
Trift08720621348290
Trift08720621346074
Trift08720621348559
Trift08720621346647
Trift08720621348702
Trift08720621348054
Trift08720621347248
Trift08720621347408
Trift08720621346715
Trift08720621360223
Trift08720621346630