Taiwan FDA registration bd0748cdeaa5edf586443629b2d27fc1
"Keystone" Surgical Guide (Non-Sterile)
TW: "金石"手術導板(未滅菌)
Taiwan·Risk Class 1·MD·KEYSTONE DENTAL, INC.·Registered Nov 30, 2017 – Nov 30, 2022CancelledRegistration details
- Analysis ID
- bd0748cdeaa5edf586443629b2d27fc1
- License Form
- Ministry of Health Medical Device Import No. 018563
- Customs Code
- DHA09401856301
Company information
- Manufacturer
- KEYSTONE DENTAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HUNG KUO MEDICAL INSTRUMENT CO., LTD.
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3980 Dental Intraosseous Implant Attachment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 30, 2017
- Expiry Date
- Nov 30, 2022
- Cancellation Date
- May 12, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Keystone" Surgical Guide (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 bd0748cdeaa5edf586443629b2d27fc1 and manufactured by KEYSTONE DENTAL, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..
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