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"Lijijing" denture adhesive (unsterilized) - Taiwan Registration 0cf27d4951a8865a05f15a3332444225

Access comprehensive regulatory information for "Lijijing" 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 0cf27d4951a8865a05f15a3332444225 and manufactured by SHEFFIELD PHARMACEUTICALS. The authorized representative in Taiwan is Xinmao Pharmaceutical Co., Ltd.

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.

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0cf27d4951a8865a05f15a3332444225
Registration Details
Taiwan FDA Registration: 0cf27d4951a8865a05f15a3332444225
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Device Details

"Lijijing" denture adhesive (unsterilized)
TW: โ€œ่މๆ—ขๆทจโ€ๅ‡็‰™้ป่‘—ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0cf27d4951a8865a05f15a3332444225

DHA04400772102

Company Information

United States

Product Details

Limited to the first level of identification scope of the "Sodium Amino Methyl Cellulose, and/or Polyethylene Methyl Ether Sodium Maleic Acid Calcium Sodium Compound Denture Adhesive (F.3490) for the Classification and Grading Management Measures for Medical Devices".

F Dentistry

F.3490 Aminomethyl fiber-vigan metal, and/or polyethylene methyl ether butylate calcium butylate calcium compound denture adhesive

import

Dates and Status

May 12, 2009

May 12, 2029