Taiwan FDA registration c702941a30b567614e39e035c2b7565a
"Chongjin" manual suction device (not sterilized)
TW: “崇仁”手動式吸引器 (未滅菌)
Taiwan·Risk Class 1·GALEMED CORPORATION·Registered Dec 17, 2012 – Dec 17, 2027ActiveRegistration details
- Analysis ID
- c702941a30b567614e39e035c2b7565a
Company information
- Manufacturer
- GALEMED CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GALEMED CORPORATION
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, tracheobronchial suction catheter (D.6810) first level identification range.
- 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
- Dec 17, 2012
- Expiry Date
- Dec 17, 2027
About this record
Access comprehensive regulatory information for "Chongjin" manual suction device (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c702941a30b567614e39e035c2b7565a and manufactured by GALEMED CORPORATION. The authorized representative in Taiwan is GALEMED 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