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Free Cyprus medical device classification tool

Describe your device and get a preliminary CYMDA risk class, a clear explanation, official source links, and similar registered products where available.

Free · no loginStructured outputOfficial source linksRegistry evidence where available

Describe your device

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Tell us what the device does, who uses it, how it contacts the body, and whether it is powered, implantable, sterile, measuring, software, or an IVD.

Preliminary informational result — not an official regulatory decision.0 / 5,000
About this classifier

What the Cyprus classifier checks

The classifier compares your product description with current CYMDA classification requirements. It then gives you a suggested class, explains why it may apply, and shows the source links and product examples behind the result.

How are medical devices classified in Cyprus?
CYMDA uses a risk-based framework. Possible classes include IVDs: IVD Class A, IVD Class B, IVD Class C, IVD Class D; Medical devices: Class I, Class Is, Class Im, Class Ir, Class IIa, Class IIb, Class III. National projection of the directly applicable EU IVDR classification. The canonical class axis and rules are maintained in eu:ivd; the Cypriot references describe only administration — the separate CYMDA registration form for in-vitro diagnostic products and the language rule, which the CYMDA applies to in-vitro diagnostic products expressly. National projection of the directly applicable EU MDR classification. The canonical class axis and rules are maintained in eu:medical-device; the Cypriot references describe only administration — the CYMDA notification duty, the language requirements, the importer-details duty and the EUDAMED registration that have to be satisfied around the Union class. The CYMDA's own definitions-and-classification page adds the remaining national finding and is folded here because the schema caps a scheme at three reference sources: the CYMDA publishes the Cypriot definition of a medical device verbatim as 'Κανονισμός (ΕΕ) 2017/745, Άρθρο 2(1)', so the national definition is the Union definition and the authority does not operate a parallel national class axis. That page is not dropped — it remains bound to this promotion as a certification official source. The three references retained here are the ones with no substitute locator: the CYMDA notification page for the operative national procedure, and the notices of 6 November 2025 and 24 March 2026, which are respectively the only retrievable locators for Decree No. 7 of 5 January 2012 and for Decree No. 6 under article 59(1)(ζ) of the Basic Requirements Laws 2002 to 2011. The applicable class depends on the product's intended purpose, duration of use, invasiveness, active functions, implantability, sterility, software role, and other market-specific rules.
What information does the Cyprus classifier use?
Current official CYMDA classification requirements. Your result includes an explanation and links to the official sources used.
Is the result an official CYMDA classification decision?
No. The result is a preliminary estimate based on the product details you provide and the information available. Confirm the classification with the applicable authority or a qualified regulatory professional before filing.
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