Taiwan FDA registration 99e4d75deb4cf4fb078a73691c7e2db2

HANNOR Intraoral gel (unsterilized)

TW: 翰諾士口內凝膠 (未滅菌)

Taiwan·Risk Class 1·Hannos Corporation (HANNOS) Co., Ltd.;; Hanqiang Biotechnology Co., Ltd·Registered Jun 14, 2019 – Jun 14, 2029Active

Registration details

Analysis ID: 99e4d75deb4cf4fb078a73691c7e2db2

Company information

Manufacturer: Hannos Corporation (HANNOS) Co., Ltd.;; Hanqiang Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HANNOX INTERNATIONAL CORP.

Product details

Intended Use: Limited to the first level identification range of the "Liquid Bandage (J.5090)" Classification and Grading Management Measures for Medical Equipment.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5090 Liquid bandages
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Jun 14, 2019
Expiry Date: Jun 14, 2029

About this record

Access comprehensive regulatory information for HANNOR 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 99e4d75deb4cf4fb078a73691c7e2db2 and manufactured by Hannos Corporation (HANNOS) Co., Ltd.;; Hanqiang Biotechnology Co., Ltd. The authorized representative in Taiwan is HANNOX INTERNATIONAL 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.