Taiwan FDA registration d3f125cdf3fb919908aabfe193b52d3b
“Rusch” Laryngoflex Tube
TW: “路希”喉頭管
Taiwan·Risk Class 2·MD·WILLY RUSCH GMBH·Registered May 01, 2014 – May 01, 2024ExpiredRegistration details
- Analysis ID
- d3f125cdf3fb919908aabfe193b52d3b
- License Form
- Ministry of Health Medical Device Import No. 026128
- Customs Code
- DHA05602612808
Company information
- Manufacturer
- WILLY RUSCH GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN 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
- Imported from abroad
Dates and status
- Registration Date
- May 01, 2014
- Expiry Date
- May 01, 2024
About this record
Access comprehensive regulatory information for “Rusch” Laryngoflex Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3f125cdf3fb919908aabfe193b52d3b and manufactured by WILLY RUSCH GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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