Taiwan FDA registration d9cf056b8b734f1a0e737bb7f6559e2c
"Kant" connecting pipe (unsterilized)
TW: "康德" 連接管 (未滅菌)
Taiwan·Risk Class 1·CODAN MEDIZINISCHE GERÄTE GMBH & CO. KG·Registered Feb 20, 2006 – Feb 20, 2016CancelledRegistration details
- Analysis ID
- d9cf056b8b734f1a0e737bb7f6559e2c
- Customs Code
- DHA04400266401
Company information
- Manufacturer
- CODAN MEDIZINISCHE GERÄTE GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- TRIPLE ROPES ENTERPRISE CO., LTD.
Product details
- Intended Use
- Used to introduce non-drug fluids into or from body cavities other than blood vessels, or to evaluate certain physiological conditions.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Feb 20, 2006
- Expiry Date
- Feb 20, 2016
- Cancellation Date
- Apr 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kant" connecting pipe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d9cf056b8b734f1a0e737bb7f6559e2c and manufactured by CODAN MEDIZINISCHE GERÄTE GMBH & CO. KG. The authorized representative in Taiwan is TRIPLE ROPES ENTERPRISE 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