Taiwan FDA registration 58bf0275fcac8d8343b1afb268d7d89f
"Spectrum" Spectragel 2Q (non-sterile)
TW: "思貝強" 疤痕凝膠 (未滅菌)
Taiwan·Risk Class 1·MD·SPECTRUM DESIGNS, INC.·Registered Mar 23, 2015 – Mar 23, 2020CancelledRegistration details
- Analysis ID
- 58bf0275fcac8d8343b1afb268d7d89f
- License Form
- Ministry of Health Medical Device Import No. 015028
- Customs Code
- DHA09401502800
Company information
- Manufacturer
- SPECTRUM DESIGNS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Beleli Biotechnology Co., Ltd
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4025 Scar Treatment Silicone Products
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 23, 2015
- Expiry Date
- Mar 23, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Spectrum" Spectragel 2Q (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 58bf0275fcac8d8343b1afb268d7d89f and manufactured by SPECTRUM DESIGNS, INC.. The authorized representative in Taiwan is Beleli Biotechnology Co., Ltd.
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