Taiwan FDA registration 0462a74be80dfa0269c487cfcb5a7f64
Crystal emulsification aspiration / vitreous excision device "Alcon"
TW: 晶體乳化吸除/玻離體切除儀〝愛爾康〞
Taiwan·ALCON MANUFACTURING, LTD.·Registered Aug 28, 1992 – Aug 28, 2007CancelledRegistration details
- Analysis ID
- 0462a74be80dfa0269c487cfcb5a7f64
- Customs Code
- DHA00600675606
Company information
- Manufacturer
- ALCON MANUFACTURING, LTD.
- Manufacturer Country
- United States
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
Product details
- Intended Use
- The details are as detailed as the approved copy of the imitation label
- Product Type (Level 1)
- 1999 Other medical coagulation devices
- Import Information
- import
Dates and status
- Registration Date
- Aug 28, 1992
- Expiry Date
- Aug 28, 2007
- Cancellation Date
- Nov 19, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Crystal emulsification aspiration / vitreous excision device "Alcon" in Taiwan's medical device market through Pure Global AI's free database. is registered under number 0462a74be80dfa0269c487cfcb5a7f64 and manufactured by ALCON MANUFACTURING, LTD.. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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