Taiwan FDA registration 605a3fa2bd53afd7009a149ea5ded4c8
"Six" hyperbaric oxygen therapy chamber
TW: “矽克斯”高壓氧氣治療艙
Taiwan·Risk Class 2·SECHRIST INDUSTRIES, INC.·Registered Aug 04, 2016 – Aug 04, 2021CancelledRegistration details
- Analysis ID
- 605a3fa2bd53afd7009a149ea5ded4c8
- Customs Code
- DHA05602875506
Company information
- Manufacturer
- SECHRIST INDUSTRIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- AIR PRODUCTS SAN FU 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 04, 2016
- Expiry Date
- Aug 04, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Six" 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 605a3fa2bd53afd7009a149ea5ded4c8 and manufactured by SECHRIST INDUSTRIES, INC.. The authorized representative in Taiwan is AIR PRODUCTS SAN FU CO., LTD..
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