Taiwan FDA registration fd03edfe25fd010c6f13d46b159e5565
"Ward" wet bottle (unsterilized)
TW: "華德" 潮濕瓶 (未滅菌)
Taiwan·Risk Class 1·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Jul 21, 2016 – Jul 21, 2026ExpiredRegistration details
- Analysis ID
- fd03edfe25fd010c6f13d46b159e5565
Company information
- Manufacturer
- HEADSTAR MEDICAL PRODUCTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HEADSTAR MEDICAL PRODUCTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Household Treatment Moisturizer (D.5460)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5460 家用治療潮濕器
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 21, 2016
- Expiry Date
- Jul 21, 2026
About this record
Access comprehensive regulatory information for "Ward" wet bottle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd03edfe25fd010c6f13d46b159e5565 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..
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