Taiwan FDA registration 5a140a36f35e72103fdd24db6ad8764f
“Vitaltec” Rota-Trach Pediatric Tracheostomy Tube
TW: “旭邦”柔得多幼兒型氣切管
Taiwan·Risk Class 2·MD·Xubang Medical Equipment Co., Ltd·Registered Feb 24, 2014 – Feb 24, 2029ActiveRegistration details
- Analysis ID
- 5a140a36f35e72103fdd24db6ad8764f
- License Form
- Ministry of Health Medical Device Manufacturing No. 004535
Company information
- Manufacturer
- Xubang Medical Equipment Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Xubang Medical Equipment Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5800 Trachetomy tube and its balloon
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 24, 2014
- Expiry Date
- Feb 24, 2029
About this record
Access comprehensive regulatory information for “Vitaltec” Rota-Trach Pediatric Tracheostomy Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a140a36f35e72103fdd24db6ad8764f and manufactured by Xubang Medical Equipment Co., Ltd. The authorized representative in Taiwan is Xubang Medical Equipment 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