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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

99010319 — IVDR Class A IVDR by Cerascreen GmbH

MD Atlas
Cerascreen GmbH

EUDAMED last updated this device on Nov 3, 2023

99010319

42516207004JV

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: 04251620704991
Reference / catalog number: 99010319

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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	May 1, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04251620704991
Basic UDI-DI: 42516207004JV
Reference / catalog number: 99010319
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® Probiotische Bakterien Test ist ein Pro-benahme- und Einsendekit für eine Stuhluntersuchungauf Laktobazillen und Bifidobakterien. Der Test dient der Bestimmung der Bakteriengattungen Lactobacillus und Bifidobacterium im Stuhl. Die Probe wird in unserem spezialisierten cerascreen® Diagnostik-Partnerlabor in vitro ausgewertet.
Additional information URL: https://cerascreen.info/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W05019001FAECES COLLECTION DEVICES

Compliance flags

Safety

Sterile

Single use

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Sterilization

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New device

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