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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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Organization name
UDI-DI code
Reference / catalog number

MT0001G — IVDR Class A IVDR by Microviable Therapeutics

MD Atlas
Microviable Therapeutics

EUDAMED last updated this device on May 12, 2026

MT0001G

8437025337MT0001G7G

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Microviable Therapeutics
UDI-DI code: 08437025337002
Reference / catalog number: MT0001G

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Manufacturer information

Organization name: Microviable Therapeutics
SRN: ES-MF-000030013
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437025337002
Basic UDI-DI: 8437025337MT0001G7G
Reference / catalog number: MT0001G
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: GutAlive® has been designed to collect and transport microbiota samples in anaerobic conditions enabling bacterial viability, including strict anaerobic bacteria, to warranty the original microbial composition and diversity.
Additional information URL: https://www.microviable.com/en/gutalive-2/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W05019001FAECES COLLECTION DEVICES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Software identification

Related devices

This device is not currently linked to any other device.

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.