Taiwan FDA registration 2a85704e88c87a1eb782459a5ee092b7
"Fuzhan Mei" respirator tubing (unsterilized)
TW: "福展美"呼吸器管路 (未滅菌)
Taiwan·Risk Class 1·Fuzhan Mei Technology Co., Ltd. Dongshan Factory·Registered Feb 16, 2015 – Feb 16, 2030ActiveRegistration details
- Analysis ID
- 2a85704e88c87a1eb782459a5ee092b7
Company information
- Manufacturer
- Fuzhan Mei Technology Co., Ltd. Dongshan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FOXXMED LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Respirator Pipeline (D.5975)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5975 Respirator Tubing
- Import Information
- Domestic
Dates and status
- Registration Date
- Feb 16, 2015
- Expiry Date
- Feb 16, 2030
About this record
Access comprehensive regulatory information for "Fuzhan Mei" respirator tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2a85704e88c87a1eb782459a5ee092b7 and manufactured by Fuzhan Mei Technology Co., Ltd. Dongshan Factory. The authorized representative in Taiwan is FOXXMED LTD..
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