Taiwan FDA registration 93f1cc30e7d5e979b71ded58d308b4b6
Lynwitt Max Electric Surgery Battery System (Unsterilized)
TW: "靈威特"麥克斯電動手術電池系統 (未滅菌)
Registration details
- Analysis ID
- 93f1cc30e7d5e979b71ded58d308b4b6
- Customs Code
- DHA04400282805
Company information
- Manufacturer
- LINVATEC CORPORATION D/B/A CONMED LINVATEC
- Manufacturer Country
- United States
- Authorized Representative
- WEECON CO., LTD.
Product details
- Intended Use
- Surgical appliances, motors and accessories are used with alternating current; Dry cell batteries, or aerodynamic devices, are intended to provide electricity during surgery to operate various accessories or accessories to cut hard or soft tissues.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4820 Surgical Appliances and Accessories or Accessories
- Import Information
- import
Dates and status
- Registration Date
- Mar 07, 2006
- Expiry Date
- Mar 07, 2011
- Cancellation Date
- Nov 01, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Lynwitt Max Electric Surgery Battery System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 93f1cc30e7d5e979b71ded58d308b4b6 and manufactured by LINVATEC CORPORATION D/B/A CONMED LINVATEC. The authorized representative in Taiwan is WEECON CO., LTD..
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