Taiwan FDA registration d7cb2d4bc7e7e3fb4c80b82eb6daccd5
"Kehao-style" Peritai Esp implant system
TW: “克浩式”培里泰艾斯普植體系統
Taiwan·Risk Class 3·CLINICAL HOUSE EUROPE GMBH·Registered May 05, 2011 – Nov 09, 2015CancelledRegistration details
- Analysis ID
- d7cb2d4bc7e7e3fb4c80b82eb6daccd5
- Customs Code
- DHA00602164905
Company information
- Manufacturer
- CLINICAL HOUSE EUROPE GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- ARCHER MEDICAL TRADING CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3640 Bone Implants
- Import Information
- import
Dates and status
- Registration Date
- May 05, 2011
- Expiry Date
- Nov 09, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kehao-style" Peritai Esp implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d7cb2d4bc7e7e3fb4c80b82eb6daccd5 and manufactured by CLINICAL HOUSE EUROPE GMBH. The authorized representative in Taiwan is ARCHER MEDICAL TRADING CORP..
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