Taiwan FDA registration f49aa5b429af254d955abb03b467e04c
“RUSCH” Extra Tracheoflex Tube and Accessories
TW: “路希”崔西歐費雷思氣切管及配件
Taiwan·Risk Class 2·MD·WILLY RUSCH GMBH·Registered Apr 27, 2015 – Apr 27, 2020CancelledRegistration details
- Analysis ID
- f49aa5b429af254d955abb03b467e04c
- License Form
- Ministry of Health Medical Device Import No. 027274
- Customs Code
- DHA05602727401
Company information
- Manufacturer
- WILLY RUSCH GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5800 Trachetomy tube and its balloon
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 27, 2015
- Expiry Date
- Apr 27, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “RUSCH” Extra Tracheoflex Tube and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f49aa5b429af254d955abb03b467e04c and manufactured by WILLY RUSCH GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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