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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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CryoPro Contact Probe — 11 UDI-DI variants, MDR

MD Atlas
Cortex Technology Aps

Data from EUDAMED, last updated May 23, 2026

CryoPro Contact Probe

5710188CONTACTWN

11 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: Cortex Technology Aps

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5710188CONTACTWN
Device name: CryoPro Contact Probe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Cortex Technology Aps
SRN: DK-MF-000002984
Country: Denmark
Email: frn@cortex.dk

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01KQYMB0RSMNEHCXQFKF7SC73Q

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

CP 1 mm05710188020619
CP 10 mm05710188020688
CP 15 mm05710188020695
CP 2 mm05710188020626
CP 20 mm05710188020701
CP 30 mm05710188020718
CP 4 mm05710188020640
CP 5 mm05710188020657
CP 6 mm05710188020664
CP 8 mm05710188020671
CP SP05710188020602