Taiwan FDA registration 0ba833f0b580a0250e589bee1bc5d04a
"Sibeqiang" nasal implants
TW: “詩貝強”鼻植入物
Taiwan·Risk Class 2·SPECTRUM DESIGNS, INC.·Registered Sep 04, 2007 – Sep 04, 2022CancelledRegistration details
- Analysis ID
- 0ba833f0b580a0250e589bee1bc5d04a
- Customs Code
- DHA00601830005
Company information
- Manufacturer
- SPECTRUM DESIGNS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Beleli Biotechnology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3680 Nasal Supplement
- Import Information
- import
Dates and status
- Registration Date
- Sep 04, 2007
- Expiry Date
- Sep 04, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Sibeqiang" nasal implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0ba833f0b580a0250e589bee1bc5d04a and manufactured by SPECTRUM DESIGNS, INC.. The authorized representative in Taiwan is Beleli Biotechnology 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