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"Selenox" hyperbaric oxygen therapy chamber - Taiwan Registration d82d48f408587f385f0d41e3b0232cea

Access comprehensive regulatory information for "Selenox" hyperbaric oxygen therapy chamber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d82d48f408587f385f0d41e3b0232cea and manufactured by SECHRIST INDUSTRIES, INC.. The authorized representative in Taiwan is SAN FU CHEMICAL CO., LTD..

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d82d48f408587f385f0d41e3b0232cea
Registration Details
Taiwan FDA Registration: d82d48f408587f385f0d41e3b0232cea
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Device Details

"Selenox" hyperbaric oxygen therapy chamber
TW: โ€œ็ก’ๅ…‹ๆ–ฏโ€้ซ˜ๅฃ“ๆฐงๆฐฃๆฒป็™‚่‰™
Risk Class 2

Registration Details

d82d48f408587f385f0d41e3b0232cea

DHA05603390302

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5470 Hyperbaric chamber

Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Aug 26, 2020

Aug 26, 2025