Taiwan FDA registration 4766be4eb063a193df88925e529e8b3c
Zhipeng Dental Diamond Instruments (Unsterilized)
TW: 智鵬 牙科用鑽石器械 (未滅菌)
Taiwan·Risk Class 1·Penglin Enterprise Co., Ltd. Wanxing Factory·Registered Oct 24, 2016 – Oct 24, 2021CancelledRegistration details
- Analysis ID
- 4766be4eb063a193df88925e529e8b3c
Company information
- Manufacturer
- Penglin Enterprise Co., Ltd. Wanxing Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Penglin Enterprise Co., Ltd. Wanxing Factory
Product details
- Intended Use
- Limited to the first level identification range of dental diamond instruments (F.4535) under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4535 牙科用鑽石器械
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 24, 2016
- Expiry Date
- Oct 24, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Zhipeng Dental Diamond Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4766be4eb063a193df88925e529e8b3c and manufactured by Penglin Enterprise Co., Ltd. Wanxing Factory. The authorized representative in Taiwan is Penglin Enterprise Co., Ltd. Wanxing Factory.
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