Taiwan FDA registration eef07b05986936aab72e3654d6482d03
"Tavik" dermabrasive (unsterilized)
TW: “塔維克”磨皮機 (未滅菌)
Taiwan·Risk Class 1·TAVTECH LTD.·Registered Sep 21, 2006 – Sep 21, 2016CancelledRegistration details
- Analysis ID
- eef07b05986936aab72e3654d6482d03
- Customs Code
- DHA04400518109
Company information
- Manufacturer
- TAVTECH LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- SERVICETECH INTERNATIONAL INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- 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
- Sep 21, 2006
- Expiry Date
- Sep 21, 2016
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Tavik" dermabrasive (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eef07b05986936aab72e3654d6482d03 and manufactured by TAVTECH LTD.. The authorized representative in Taiwan is SERVICETECH INTERNATIONAL INC..
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