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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

LetsGetChecked Stool Home Sample… — IVDR Class A IVDR

MD Atlas
PrivaPath Diagnostics Limited

EUDAMED last updated this device on Apr 8, 2026

LetsGetChecked Stool Home Sample Collection Kit

850024881SCT6

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: PrivaPath Diagnostics Limited
UDI-DI code: 00850024881259
Reference / catalog number: FT01I

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Manufacturer information

Organization name: PrivaPath Diagnostics Limited
SRN: IE-MF-000045162
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Ireland; available across 1 country total.

Country	On market since	Until
IrelandPrimary placement		Still on market

Device identification

Trade name: LetsGetChecked Stool Home Sample Collection Kit
UDI-DI code: 00850024881259
Basic UDI-DI: 850024881SCT6
Reference / catalog number: FT01I
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: The LetsGetChecked Stool Home Sample Collection Kit is an in vitro diagnostic medical device specifically intended for the primary containment and preservation of stool samples, for the purpose of in vitro diagnostic examination by our partner laboratories.
Additional information URL: No additional information URL provided by the manufacturer.
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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.

Related devices

This device is not currently linked to any other device.