Taiwan FDA registration 36b94e0e32dc90461d2be8ab318f7b64
"Zhipeng" tooth intraosseous implant attachment (unsterilized)
TW: "智鵬"牙齒骨內植入物附件(未滅菌)
Taiwan·Risk Class 1·Penglin Enterprise Co., Ltd. Wanxing Factory·Registered Apr 08, 2013 – Apr 08, 2023ExpiredRegistration details
- Analysis ID
- 36b94e0e32dc90461d2be8ab318f7b64
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 scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3980 Intradental implant manipulation equipment
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 08, 2013
- Expiry Date
- Apr 08, 2023
About this record
Access comprehensive regulatory information for "Zhipeng" tooth intraosseous implant attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 36b94e0e32dc90461d2be8ab318f7b64 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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