Taiwan FDA registration b18e1b9b69d428801b863494bcc00646
"Kjeldahl" scalpel
TW: 〝凱氏〞手術刀
Taiwan·Risk Class 1·KAI INDUSTRIES CO., LTD.·Registered Nov 21, 2005 – Nov 21, 2010CancelledRegistration details
- Analysis ID
- b18e1b9b69d428801b863494bcc00646
- Customs Code
- DHA04400205808
Company information
- Manufacturer
- KAI INDUSTRIES CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- HORIZON INSTRUMENTS CO. ,LTD.
Product details
- Intended Use
- Hand-held or hand-operated blades or knife handles, discarded immediately after use, are used in a variety of general operations.
- 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
- Nov 21, 2005
- Expiry Date
- Nov 21, 2010
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kjeldahl" scalpel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b18e1b9b69d428801b863494bcc00646 and manufactured by KAI INDUSTRIES CO., LTD.. The authorized representative in Taiwan is HORIZON INSTRUMENTS 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