Taiwan FDA registration ea4f1e0e9eef543905f96d4d0736790d
"Interve" dental implant surgical instruments (unsterilized)
TW: “英特崴” 植牙手術器械(未滅菌)
Taiwan·Risk Class 1·Bomei Co., Ltd.;; Intervin Co., Ltd·Registered Apr 24, 2023 – Apr 24, 2028ActiveRegistration details
- Analysis ID
- ea4f1e0e9eef543905f96d4d0736790d
Company information
- Manufacturer
- Bomei Co., Ltd.;; Intervin Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- INTEWARE CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, dental handsets and their accessories (F.4200) first-level identification range.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4200 Dental handset and accessories thereof
- Import Information
- 國產;; 委託製造;; QMS/QSD
Dates and status
- Registration Date
- Apr 24, 2023
- Expiry Date
- Apr 24, 2028
About this record
Access comprehensive regulatory information for "Interve" dental implant surgical 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 ea4f1e0e9eef543905f96d4d0736790d and manufactured by Bomei Co., Ltd.;; Intervin Co., Ltd. The authorized representative in Taiwan is INTEWARE CO., LTD..
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