Taiwan FDA registration 67f05015b4215d934bfcc180d889001a
“Kerr” Herculite Précis Flow
TW: “科爾”賀萊斯流動性修復材料
Taiwan·Risk Class 2·MD·KERR CORPORATION·Registered Oct 21, 2019 – Oct 21, 2024ExpiredRegistration details
- Analysis ID
- 67f05015b4215d934bfcc180d889001a
- License Form
- Ministry of Health Medical Device Import No. 032869
- Customs Code
- DHA05603286900
Company information
- Manufacturer
- KERR CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- NOBEL BIOCARE TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 21, 2019
- Expiry Date
- Oct 21, 2024
About this record
Access comprehensive regulatory information for “Kerr” Herculite Précis Flow in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67f05015b4215d934bfcc180d889001a and manufactured by KERR CORPORATION. The authorized representative in Taiwan is NOBEL BIOCARE TAIWAN CO., LTD..
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