Taiwan FDA registration ff6bedc885ba4da7d9d86fd93624fbd8
"Xinfeng" Suction catheter and suction kit (sterilized)
TW: "新豐" 吸引導管及吸痰包(滅菌)
Registration details
- Analysis ID
- ff6bedc885ba4da7d9d86fd93624fbd8
- Customs Code
- DHY04300003100
Company information
- Manufacturer
- SYMPHON MEDICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SYMPHON MEDICAL TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Liquid or semi-solid secretions are removed from the patient's upper airway.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- Domestic
Dates and status
- Registration Date
- May 16, 2005
- Expiry Date
- May 16, 2025
About this record
Access comprehensive regulatory information for "Xinfeng" Suction catheter and suction kit (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ff6bedc885ba4da7d9d86fd93624fbd8 and manufactured by SYMPHON MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SYMPHON MEDICAL TECHNOLOGY 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