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Health Products
Health Products
| 301 | Re: Medical device import facilities, B.E. 2552 (2009) |
| 302 | Re: Classes of medical devices or medical devices for which manufacturers or importers are required to obtain a license, B.E. 2563 (2020) |
| 303 | Re: Classes of medical devices or medical devices in respect of which manufacturers or importers are required to make a notification, B.E. 2563 (2020) |
| 304 | Re: Rules, procedures and conditions on display of labels and medical device package inserts, B.E. 2563 (2020) |
| 305 | Re: Rules, procedures and conditions for preparation of reports on medical device malfunctions or adverse events occurring to consumers and reports on field safety corrective actions for medical devices, B.E. 2563 (2020) |
| 306 | Re: Risk classification of medical devices, B.E. 2562 (2019) |
| 307 | Re: Classes of medical devices or medical devices of which manufacturers or importers are required to declare specifications (no. 2), B.E. 2563 (2020) |
| 308 | Re: Prescribing rules, procedures and conditions on registration of medical device manufacturing establishments, B.E. 2552 (2009) |
| 309 | Re: Specification of standards and evaluation of test kits and reagents related to diagnosis of sars-cov-2 (virus causing covid-19) infection, B.E. 2564 (2021) |
| 310 | Cosmetics Act (No.2), B.E. 2565 (2022) |