Taiwan FDA registration d82d48f408587f385f0d41e3b0232cea
"Selenox" hyperbaric oxygen therapy chamber
TW: “硒克斯”高壓氧氣治療艙
Taiwan·Risk Class 2·SECHRIST INDUSTRIES, INC.·Registered Aug 26, 2020 – Aug 26, 2025ExpiredRegistration details
- Analysis ID
- d82d48f408587f385f0d41e3b0232cea
- Customs Code
- DHA05603390302
Company information
- Manufacturer
- SECHRIST INDUSTRIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- SAN FU CHEMICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5470 Hyperbaric chamber
- Import Information
- 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
- Registration Date
- Aug 26, 2020
- Expiry Date
- Aug 26, 2025
About this record
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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