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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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CoreTherm Catheter Standard — 2 UDI-DI variants, MDR (ProstaLund AB)

MD Atlas
ProstaLund AB

Data from EUDAMED, last updated May 31, 2026

CoreTherm Catheter Standard

0735008191CA804X20Q8

2 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: ProstaLund AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0735008191CA804X20Q8
Device name: CoreTherm Catheter Standard
Device model: CA804220
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: ProstaLund AB
SRN: SE-MF-000004428
Country: Sweden
Email: ulrika.hjellstrom.nilsson@prostalund.com
Phone: +46706720112

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KPMW9A4X6PC6ZG0A1HZ8W62P

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

CA80422007350081910051
CA80412007350081910082