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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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Stool Collection Kit (SCK) — 3 UDI-DI variants, IVDR (GOODGUT, SLU)

MD Atlas
GOODGUT, SLU

Data from EUDAMED, last updated May 23, 2026

Stool Collection Kit (SCK)

8437023437SCKAT

3 UDI-DI variants

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: GOODGUT, SLU

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437023437SCKAT
Device name: Stool Collection Kit (SCK)
Device model: Stool Collection Kit (SCK-CRC)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Sep 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: GOODGUT, SLU
SRN: ES-MF-000000229
Country: Spain
Email: info@goodgut.eu
Phone: +34 972 18 32 20

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HA9ATHHGB5YVHZZBH272Y502

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

SCK-04-CRC-es08437023437070
SCK-04-DX-es08437023437087
SCK-04-TUG-es08437023437100