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"Giushi" intraoral gel (unsterilized) - Taiwan Registration 66038b56f86da60951b95e0ef59d82c7

Access comprehensive regulatory information for "Giushi" intraoral gel (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 66038b56f86da60951b95e0ef59d82c7 and manufactured by BIOKOSMES S.R.L.; BMG PHARMA S.R.L.. The authorized representative in Taiwan is SHINER PHARM CORP..

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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66038b56f86da60951b95e0ef59d82c7
Registration Details
Taiwan FDA Registration: 66038b56f86da60951b95e0ef59d82c7
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Device Details

"Giushi" intraoral gel (unsterilized)
TW: โ€œๅ‰ๅ„ช้ฉโ€ๅฃๅ…งๅ‡่† (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

66038b56f86da60951b95e0ef59d82c7

DHA09401409000

Company Information

Product Details

Limited to the first level identification range of the "Liquid Bandage (J.5090)" Classification and Grading Management Measures for Medical Equipment.

J General hospital and personal use equipment

J.5090 Liquid bandages

Contract manufacturing;; input

Dates and Status

Apr 25, 2014

Apr 25, 2024