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The Food and Drug Administration (FDA) informs the public that the advisory on the medical device product “Indoplas Infrared Ear Thermometer” under FDA Advisory No. 2018-120 dated 02 April 2018 is hereby lifted pursuant to the compliance of the market authorization holder to existing and applicable laws, rules, and regulations.

The above-mentioned medical device product is REGISTERED with Certificate of Product Registration No. MDR-06882 valid until 29 June 2019 under company Indoplas Philippines, Inc.

The issuance of this advisory shall not in any manner preclude this Office from issuing subsequent orders it may deem necessary and appropriate, should there be findings of any violation of the company to existing laws, rules, and regulations.

For more information and inquiries, please e-mail us at info@fda.gov.ph or call the Center for Device Regulation, Radiation Health, and Research at (02) 857-1900 local 8301. To report sale or distribution of any unregistered medical device products, kindly email us via report@fda.gov.ph.

FDA Advisory No. 2018-237