Taiwan FDA registration cff69fb3eeb05057682599fa7400b32c
Zhipeng light curing machine
TW: 智鵬光固化機
Taiwan·Risk Class 2·Penglin Enterprise Co., Ltd. Wanxing Factory·Registered Oct 12, 2007 – Oct 12, 2022CancelledRegistration details
- Analysis ID
- cff69fb3eeb05057682599fa7400b32c
- Customs Code
- DHY00500228202
Company information
- Manufacturer
- Penglin Enterprise Co., Ltd. Wanxing Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PENG LIM ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.6070 Ultraviolet Activator for Polymerization
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 12, 2007
- Expiry Date
- Oct 12, 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 Zhipeng light curing machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cff69fb3eeb05057682599fa7400b32c and manufactured by Penglin Enterprise Co., Ltd. Wanxing Factory. The authorized representative in Taiwan is PENG LIM ENTERPRISE CO., LTD..
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