Taiwan FDA registration ae203b102f6cf26e826a731dfbece401

"Meta" Gutta Percha Points (Non-Sterile)

TW: "麥塔" 馬來膠 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·META BIOMED CO., LTD.·Registered Apr 12, 2019 – Apr 12, 2024Expired
Registration details
Analysis ID
ae203b102f6cf26e826a731dfbece401
License Form
Ministry of Health Medical Device Import No. 020305
Customs Code
DHA09402030507
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
UNIGLIFE BIOMED CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F3850 Male-Glue
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 12, 2019
Expiry Date
Apr 12, 2024
Companies making similar products

Top companies providing products similar to ""Meta" Gutta Percha Points (Non-Sterile)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Meta" Gutta Percha Points (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ae203b102f6cf26e826a731dfbece401 and manufactured by META BIOMED CO., LTD.. The authorized representative in Taiwan is UNIGLIFE BIOMED CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including META BIOMED CO., LTD., and 1 recent registrations in the same category. 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+ Devices1 Competitors1 Recent Registrations