Taiwan FDA registration 6b6bcdd6bc9c01ff4b492e79b95d9bf6
“HearMEC” AirForce Hyperbaric Oxygen Chamber O2 Prime Cabin
TW: “哈美克” 溫和高壓氧艙
Taiwan·Risk Class 2·MD·HEARMEC CO., LTD.·Registered Oct 10, 2022 – Oct 10, 2027ActiveRegistration details
- Analysis ID
- 6b6bcdd6bc9c01ff4b492e79b95d9bf6
- License Form
- Ministry of Health Medical Device Import No. 035959
- Customs Code
- DHA05603595900
Company information
- Manufacturer
- HEARMEC CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Health Way Biomedical Co., Ltd.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D5470 Hyperbaric oxygen chamber
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 10, 2022
- Expiry Date
- Oct 10, 2027
About this record
Access comprehensive regulatory information for “HearMEC” AirForce Hyperbaric Oxygen Chamber O2 Prime Cabin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b6bcdd6bc9c01ff4b492e79b95d9bf6 and manufactured by HEARMEC CO., LTD.. The authorized representative in Taiwan is Health Way Biomedical Co., Ltd..
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