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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 SE — 1 UDI-DI variant, MDD (ProstaLund AB)

MD Atlas
ProstaLund AB

Data from EUDAMED, last updated May 31, 2026

CoreTherm SE

B-07350081910204

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: ProstaLund AB

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: G10 080865 0012
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TÜV SÜD Product Service GmbH (0123)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-07350081910204
Device name: CoreTherm SE
Device model: PLC802600
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 18, 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

1 UDI-DI variant

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Applied filters

basicUdiUlid01KRXF0KQ1MDEWKHMGJPK4YSK1

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

PLC80260007350081910204