Taiwan FDA registration 86d6f92a374e3ca277a123d733d359d5
"Bantron" glass fiber reinforced root column retention system (unsterilized)
TW: "班特朗"玻璃纖維強化根柱固位系統(未滅菌)
Taiwan·Risk Class 1·PENTRON CLINICAL TECHNOLOGIES, LLC·Registered Nov 22, 2005 – Nov 22, 2010CancelledRegistration details
- Analysis ID
- 86d6f92a374e3ca277a123d733d359d5
- Customs Code
- DHA04400206202
Company information
- Manufacturer
- PENTRON CLINICAL TECHNOLOGIES, LLC
- Manufacturer Country
- United States
- Authorized Representative
- Maojie Industrial Co., Ltd
Product details
- Intended Use
- This device is made of Austenitic alloy or more than 75% gold and platinum group metals, which is used to bond to the root of the tooth to stabilize and support the complex.
- Product Type (Level 1)
- F Dentistry
- Import Information
- import
Dates and status
- Registration Date
- Nov 22, 2005
- Expiry Date
- Nov 22, 2010
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bantron" glass fiber reinforced root column retention system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 86d6f92a374e3ca277a123d733d359d5 and manufactured by PENTRON CLINICAL TECHNOLOGIES, LLC. The authorized representative in Taiwan is Maojie Industrial Co., Ltd.
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