Taiwan FDA registration 5aba5e24be955c7bfd8698151f4640b4
"Peres" water laser
TW: "百雷士" 水雷射
Taiwan·Risk Class 2·BIOLASE TECHNOLOGY, INC.·Registered Jan 25, 2006 – Aug 12, 2008CancelledRegistration details
- Analysis ID
- 5aba5e24be955c7bfd8698151f4640b4
- Customs Code
- DHA00601594204
Company information
- Manufacturer
- BIOLASE TECHNOLOGY, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Yashi Biotechnology Co., Ltd
Product details
- Intended Use
- Gum removal and cavity treatment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Jan 25, 2006
- Expiry Date
- Aug 12, 2008
- Cancellation Date
- Oct 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Peres" water laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5aba5e24be955c7bfd8698151f4640b4 and manufactured by BIOLASE TECHNOLOGY, INC.. The authorized representative in Taiwan is Yashi Biotechnology Co., Ltd.
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