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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

99010594 — IVDR Class A IVDR by Cerascreen GmbH

MD Atlas
Cerascreen GmbH

EUDAMED last updated this device on Nov 1, 2023

99010594

42516207002JR

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Cerascreen GmbH
UDI-DI code: 04251620710138
Reference / catalog number: 99010594

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Manufacturer information

Organization name: Cerascreen GmbH
SRN: DE-MF-000017602
Manufacturer status: Active

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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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Oct 19, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04251620710138
Basic UDI-DI: 42516207002JR
Reference / catalog number: 99010594
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: Der cerascreen® Vitamin D Test ist ein Probenahme-und Einsendekit zur Ermittlung des Vitamin D-Spiegels. Der Test dient der Konzentrationsbestimmung von 25-OH-Vitamin-D3 in humanem Kapillarblut. Die Probe wird in unserem spezialisierten cerascreen® Diagnostik-Partnerlabor ausgewertet. 25-OH Vit D3 25-OH Vit D2 24,25-OH 2 D3 Total Vit D (D3 and D2) 25(OH)D3:24,25 (OH)2 D3
Additional information URL: https://cerascreen.info/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0501010201CAPILLARY BLOOD COLLECTION SYSTEMS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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