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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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ReSCape — 1 UDI-DI variant, IVDR (Coris BioConcept)

MD Atlas
Coris BioConcept

Data from EUDAMED, last updated May 23, 2026

ReSCape

54200719S10024F

1 UDI-DI variant

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Coris BioConcept

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 54200719S10024F
Device name: ReSCape
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: Coris BioConcept
SRN: BE-MF-000024520
Country: Belgium
Email: info@corisbio.com
Phone: +32 (0)81 719 917

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GXWTQZ4VCWYBB7GYQZY3SSP6

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

S-100215420071900788