Taiwan FDA registration fbd5563f85c1fd28687698052bfe2842
“Headstar” Water trap (Non-sterile)
TW: “華德”集水器(未滅菌)
Registration details
- Analysis ID
- fbd5563f85c1fd28687698052bfe2842
- License Form
- Ministry of Health Medical Device Manufacturing No. 007594
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 "T-shaped drainage (water collector) (D.5995)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5995 T-drain (water collector)
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 04, 2019
- Expiry Date
- Jan 04, 2024
About this record
Access comprehensive regulatory information for “Headstar” Water trap (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fbd5563f85c1fd28687698052bfe2842 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..
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