
Free Mozambique medical device classification tool
Describe your device and get a preliminary ANARME, IP 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 Mozambique classifier checks
The classifier compares your product description with current ANARME, IP 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 Mozambique?
- ANARME, IP uses a risk-based framework. Possible classes include Medical devices: Class A, Class B, Class C, Class D; IVDs: Class A, Class B, Class C, Class D. Section 3 distinguishes low, medium, high and maximum device risk and references the local classification annex. Registration also depends on the periodically published priority list; class A and non-priority B-D products follow notification. This source check does not establish current priority-list membership. Section 3 gives a distinct IVD risk table and intended-use, user-knowledge, diagnostic-information and public-health criteria. A-D labels do not imply a Roman-numeral equivalence. Registration versus notification also depends on priority-list membership. 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 Mozambique classifier use?
- Current official ANARME, IP classification requirements. Your result includes an explanation and links to the official sources used.
- Is the result an official ANARME, IP 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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