Taiwan FDA registration 701eeff2a18c1d85ad50cbde08040fc8
"Speed" serpentine tube (unsterilized)
TW: “飛速”蛇型管(未滅菌)
Registration details
- Analysis ID
- 701eeff2a18c1d85ad50cbde08040fc8
- Customs Code
- DHA09600416107
Company information
- Manufacturer
- Shenzhonghai Medical Inc.;; AOK Tooling Ltd.
- Manufacturer Country
- Hong Kong;;China
- Authorized Representative
- AOK MEDTECH INC.
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
- Input;; Contract manufacturing;; Chinese goods
Dates and status
- Registration Date
- May 04, 2020
- Expiry Date
- May 04, 2025
About this record
Access comprehensive regulatory information for "Speed" serpentine tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 701eeff2a18c1d85ad50cbde08040fc8 and manufactured by Shenzhonghai Medical Inc.;; AOK Tooling Ltd.. The authorized representative in Taiwan is AOK MEDTECH INC..
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