Taiwan FDA registration 6063c692c3c00f3f9f85fc748762fdf0

"Kobayashi" denture adhesive (unsterilized)

TW: “小林”假牙黏著劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·KOBAYASHI PHARMACEUTICAL CO., LTD.·Registered Jun 23, 2009 – Jun 23, 2014Cancelled
Registration details
Analysis ID
6063c692c3c00f3f9f85fc748762fdf0
Customs Code
DHA04400784708
Company information
Manufacturer Country
Japan
Authorized Representative
Xile Enterprises Limited
Product details
Intended Use
Limited to the first grade identification range of the Measures for the Administration of Medical Devices "ethylene oxide polymer and/or sodium carboxymethylcellulose denture adhesive (F.3410)".
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.3410 Ethylene oxide polymer and/or carboxymethyl fibervetinol denture adhesive
Import Information
import
Dates and status
Registration Date
Jun 23, 2009
Expiry Date
Jun 23, 2014
Cancellation Date
Jul 02, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Kobayashi" denture adhesive (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6063c692c3c00f3f9f85fc748762fdf0 and manufactured by KOBAYASHI PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is Xile Enterprises Limited.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices