Taiwan FDA registration 079bf31c73bc75a54bd62bff0bd772bd
"Yuanmao" non-powered, single patient use, portable suction device (unsterilized)
TW: “遠貿”非動力式,單一病人使用,可攜帶式之抽吸器具 (未滅菌)
Registration details
- Analysis ID
- 079bf31c73bc75a54bd62bff0bd772bd
Company information
- Manufacturer
- Yuanmao Enterprise Co., Ltd. National Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FOREMOUNT ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Oct 07, 2019
- Expiry Date
- Oct 07, 2029
About this record
Access comprehensive regulatory information for "Yuanmao" non-powered, single patient use, portable suction device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 079bf31c73bc75a54bd62bff0bd772bd and manufactured by Yuanmao Enterprise Co., Ltd. National Factory. The authorized representative in Taiwan is FOREMOUNT ENTERPRISE 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