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ANNEX I TO DECLARATION OF CONFORMITY

ANNEX I TO DECLARATION OF CONFORMITY

ANNEX I TO DECLARATION OF CONFORMITY

Product catalog summary
Declaration of Conformity Overview
Product Information: The document pertains to the Microreader II, an in vitro diagnostic device. The Basic UDI-DI is 42520204MR2NY. Variants of this product are included in the declaration.
Manufacturer Details: The manufacturer is opTricon GmbH, located at Schwarzschildstr.1, 12489 Berlin, Germany. The SRN for EUDAMED is DE-MF-000024656.
Manufacturer's Responsibility: The manufacturer declares sole responsibility for issuing the EU Declaration of Conformity.
Device Purpose: The Microreader II is a photometer intended for qualitative, semi-quantitative, or quantitative measurement of optical density on test strips used in Lateral Flow Assays (LFAs) for in vitro diagnostics. It assists in diagnosing specific conditions based on tests defined by assay reagent manufacturers. The device is used manually by professional users and is not a companion diagnostic device.
Classification: According to the In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR), the device is classified as Class A, Annex VIII, Rule 5 b.
Compliance: The device complies with all applicable requirements of the IVDR (EU) 2017/746.
Technical Specifications and Assessment: No common technical specifications have been published yet. The conformity assessment procedure follows (EU) 2017/746 (IVDR); Article 17 & Annex II, Annex III. No notified body was consulted.
Signatory: The document is signed by the Managing Director of opTricon GmbH in Berlin on 2025-02-07.
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Catalog excerpts

ANNEX I TO DECLARATION OF CONFORMITY-1

Handelsname Produkt: Microreader II Trade name product: Basic UDI-DI: Die folgenden Varianten des o.g. Produktes sind in der Konformitatserklarung eingeschlossen. T HE FOLLOWING VARIANTS OF THE ABOVE-MENTIONED PRODUCT ARE INCLUDED IN THE DECLARATION OF CONFORMITY. Ort, Datum / Place, date Name und Funktion bei opTricon GmbH / Name and function at opTricon GmbH

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ANNEX I TO DECLARATION OF CONFORMITY-2

KONFORMITÄTSERKLÄRUNG / DECLARATION OF CONFORMITY Name und Adresse des Herstellers: Name and address of the Manufacturer: opTricon GmbH Schwarzschildstr.1 12489 Berlin Germany SRN des Herstellers (EUDAMED): SRN of the Manufacturer (EUDAMED): DER HERSTELLER ERKLÄRT HIERMIT, DASS ER DIE ALLEINIGE VERANTWORTUNG FÜR DIE AUSSTELLUNG DER EUKONFORMITÄTSERKLÄRUNG TRÄGT. THE MANUFACTURER HEREBY DECLARES THAT HE IS SOLELY RESPONSIBLE FOR ISSUING THE EU DECLARATION OF CONFORMITY. DER HERSTELLER ERKLÄRT WEITERHIN, DASS DAS IN-VITRO-DIAGNOSTIKUM: THE MANUFACTURER FURTHER STATES THAT THE IN VITRO DIAGNOSTIC...

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ANNEX I TO DECLARATION OF CONFORMITY-3

UND ALLEN ANFORDERUNGEN DER VERORDNUNG ÜBER IN-VITRO-DIAGNOSTIKA (EU) 2017/746 (IVDR) ENTSPRICHT, DIE ANWENDBAR SIND. AND COMPLIES WITH ALL REQUIREMENTS OF THE IN VITRO DIAGNOSTIC MEDICAL DEVICES REGULATION (EU) 2017/746 (IVDR) THAT APPLY. Angewandte Gemeinsame Technische Spezifikationen: Applied common technical specifications: N/A (bisher keine veröffentlicht / none published yet) Konformitätsbewertungsverfahren: Conformity assessment procedure: (EU) 2017/746 (IVDR); Art. 17 & Annex II, Annex III Konformitätsbewertungsstelle (falls beigezogen): Notified Body (if consulted): Unterschrift: Signature:...

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