Taiwan FDA registration 2184d86d7d908466c123f93bfce548d0
"Limei" porous tantalum metal artificial tooth root
TW: “力美”多孔鉭金屬人工牙根
Taiwan·Risk Class 3·ZIMMER DENTAL, INC.; BIOMET 3I, LLC·Registered Aug 18, 2022 – Aug 18, 2027ActiveRegistration details
- Analysis ID
- 2184d86d7d908466c123f93bfce548d0
- Customs Code
- DHA05603574800
Company information
- Manufacturer
- ZIMMER DENTAL, INC.; BIOMET 3I, LLC
- Manufacturer Country
- United States
- Authorized Representative
- HOWSHINE ENTERPRISE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3640 Bone Implants
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Aug 18, 2022
- Expiry Date
- Aug 18, 2027
About this record
Access comprehensive regulatory information for "Limei" porous tantalum metal artificial tooth root in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2184d86d7d908466c123f93bfce548d0 and manufactured by ZIMMER DENTAL, INC.; BIOMET 3I, LLC. The authorized representative in Taiwan is HOWSHINE ENTERPRISE CO., LTD..
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