PROJECT NOTES · GLOBAL MED DEVICE REGISTRY
medregdata.com
MedRegData brings medical device registration data from separate regulators into one place, then cleans, translates, and links it. One search box shows who registered which product in which country, and which companies are connected.
Registration data is more than a compliance file. It is a map for reading a market and finding an opening. This page is for companies taking products abroad: see the rules, the path, the competitors, and who is already selling there before talking about cost, timing, and the next step.
Look up equivalent devices, compare classification and approval paths across countries, find predicate products you can cite, and judge which route fits. Registration time and cost can be estimated before filing, instead of discovering the wrong path during submission.
Search a product term to find similar devices worldwide, plus importers, distributors, and authorized representatives — a background check on the compliant downstream customers. The data shows who sells a competitor’s product in each country, who they sell to, and which certificates have expired or are about to. That turns alternatives and downstream channels into a list, so outreach has a basis and a cold visit is no longer only a guess.
Use the classification code and intended use to find approved benchmark products, and read their technical characteristics and scope. Early projects wander less, and design inputs stay closer to solutions regulators have already accepted.
Take a full view of the data. Count approvals and company distribution by country, category, and time, and read the landscape from compliance records rather than hearsay. When entering a new market or setting the year’s plan, the basis can be traced back to the source.
Group similar products and their manufacturers under one product term, and at the same time see competitor coverage plus the OEMs and suppliers of those products. Competitor analysis and supply-chain selection can happen in the same search.
Search by product name, classification code, or intended use for manufacturers already approved in the target market, and the certified products those approvals cover. The records show which suppliers are compliant and whether the certificates are still valid.
Counts are from the medregdata.com homepage on 18 October 2026: 10,115,658 records (10.11 million). Coverage follows that snapshot and moves as each regulator updates.
| Market | Source | Records | What is included |
|---|---|---|---|
| United States | FDA | 426,601 | 510(k), PMA, listing, De Novo, product classification, and related databases |
| European Union | CE/EUDAMED | 2,785,689 | EUDAMED merged and deduplicated with member-state databases |
| Italy | RDM | 2,425,862 | Ministry of Health device-database snapshot |
| China | NMPA | 135,690 | NMPA medical device registration records |
| Australia | TGA ARTG | 98,554 | Australian Register of Therapeutic Goods |
| Canada | Health Canada | 153,183 | MDALL device licences |
| United Kingdom | MHRA | 1,541,151 | UK device product records |
| Singapore | HSA | 1,164,557 | Health Sciences Authority product records |
| India | CDSCO | 97,299 | Approved device records |
| Saudi Arabia | SFDA | 178,923 | Medical device product records |
| Brazil | ANVISA | 99,327 | National health surveillance records |
| Russia | RZN | 80,943 | Russian source text, with English translations |
| Japan | PMDA | 14,378 | PMDA device records |
| Israel | AMAR | 29,681 | Ministry of Health registration records |
| Thailand | Thai FDA | 570,126 | Public licence search, with English translations |
| Argentina | ANMAT | 28,753 | Device registration records |
| Mexico | COFEPRIS | 21,630 | Sanitary registrations from yearly issued-device files |
| Uzbekistan | Uzpharm | 6,571 | National register of devices and IVDs |
| Taiwan | TFDA | 93,348 | Licences from the FDA open-data export |
| Philippines | FDA | 30,340 | CPR and CMDN product authorizations |
| Indonesia | Kemenkes | 83,135 | AKD/AKL licences from e-Info Alkes |
| Malaysia | MDA | 49,917 | Active registrations from the public register |
MFDS (Korea), BfArM (Germany), and Swissmedic are marked Coming soon on the site and are not included in the counts above.
One search across the databases, plus a dedicated library for each country.
Type these in the search box. An English name works, and so does a name in another language.
United States FDA, EU CE, China NMPA, Australia TGA, and Canada.
MHRA, HSA, CDSCO, SFDA, and ANVISA.
PMDA, AMAR, and ANMAT.
Roszdravnadzor (RZN).
Thailand public licence search and Mexico sanitary registrations.
Uzpharm device and IVD register.
Extracted and loaded 134,757 CE certificate PDFs into the CE library.
PMA and 510(k)-exempt listing.
Italy RDM, Taiwan TFDA, the Philippines, Indonesia, and Malaysia.
medregdata.com is live. The databases already included can be searched from one box. More databases are still being cleaned and loaded.
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MedRegData is not affiliated with the FDA, the European Commission, NMPA, PMDA, TGA, or other regulators. Records are for reference only. As of 2026-10-18.