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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

TimeTeller® – Your Circadian Rhythm — IVDR Class A IVDR

MD Atlas
TimeTeller GmbH

EUDAMED last updated this device on May 5, 2026

TimeTeller® – Your Circadian Rhythm

426250276circadian-kit6H

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: TimeTeller GmbH
UDI-DI code: 04262502760004
Reference / catalog number: 4262502760004

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Manufacturer information

Organization name: TimeTeller GmbH
SRN: DE-MF-000044816
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Oct 28, 2025	Still on market

Device identification

Trade name: TimeTeller® – Your Circadian Rhythm
UDI-DI code: 04262502760004
Basic UDI-DI: 426250276circadian-kit6H
Reference / catalog number: 4262502760004
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 TimeTeller® Saliva Sampling Test-Kit is a sample collection and return kit intended for the collection, stabilization, and transport of human saliva samples for laboratory analysis and determination of the circadian profile.
Additional information URL: https://www.timeteller-health.com/en
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W05019002SALIVA COLLECTION DEVICES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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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.