Taiwan FDA registration 2492a5f4710bc9b643ae9a08392e6e70
"Hamek" hyperbaric oxygen chamber
TW: “哈美克”高壓氧艙
Taiwan·Risk Class 2·HEARMEC CO., LTD.·Registered Jun 19, 2020 – Jun 19, 2025ExpiredRegistration details
- Analysis ID
- 2492a5f4710bc9b643ae9a08392e6e70
- Customs Code
- DHA05603377200
Company information
- Manufacturer
- HEARMEC CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Health Way Biomedical 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
- Jun 19, 2020
- Expiry Date
- Jun 19, 2025
About this record
Access comprehensive regulatory information for "Hamek" hyperbaric oxygen chamber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2492a5f4710bc9b643ae9a08392e6e70 and manufactured by HEARMEC CO., LTD.. The authorized representative in Taiwan is Health Way Biomedical Co., Ltd..
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