Taiwan FDA registration 4f2eb714869d8ef9efdfdc2e81c88872
Master Wen Household Therapeutic Moisturist (Unsterilized)
TW: 溫大師 家用治療潮濕器 (未滅菌)
Taiwan·Risk Class 1·Qiaolian Technology Co., Ltd. Nankan Factory·Registered Dec 27, 2012 – Dec 27, 2022CancelledRegistration details
- Analysis ID
- 4f2eb714869d8ef9efdfdc2e81c88872
Company information
- Manufacturer
- Qiaolian Technology Co., Ltd. Nankan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOCARE CORPORATION
Product details
- Intended Use
- Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Household Treatment Moisturizer (D.5460)".
- 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
- Dec 27, 2012
- Expiry Date
- Dec 27, 2022
- Cancellation Date
- Oct 20, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Master Wen Household Therapeutic Moisturist (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4f2eb714869d8ef9efdfdc2e81c88872 and manufactured by Qiaolian Technology Co., Ltd. Nankan Factory. The authorized representative in Taiwan is BIOCARE CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices