Taiwan FDA registration 670f1af5c648de13a80a071f8d6c207e
"zebris" Jaw tracking device (Non-Sterile)
TW: "薩博司" 頷骨輪廓標記裝置 (未滅菌)
Taiwan·Risk Class 1·MD·ZEBRIS MEDICAL GMBH·Registered Jan 29, 2019 – Jan 29, 2024ExpiredRegistration details
- Analysis ID
- 670f1af5c648de13a80a071f8d6c207e
- License Form
- Ministry of Health Medical Device Import No. 020077
- Customs Code
- DHA09402007707
Company information
- Manufacturer
- ZEBRIS MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BIOCARE TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Jaw Contour Marking Device (F.2060) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F2060 Jaw contour marking device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 29, 2019
- Expiry Date
- Jan 29, 2024
About this record
Access comprehensive regulatory information for "zebris" Jaw tracking device (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 670f1af5c648de13a80a071f8d6c207e and manufactured by ZEBRIS MEDICAL GMBH. The authorized representative in Taiwan is BIOCARE TECHNOLOGY CO., LTD..
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