Taiwan FDA registration 322e0b5e6a9633ce02888ed6ac182265

"Changxin Seigi" occlusal paper (unsterilized)

TW: "長欣生技" 咬合紙 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·TIANJIN SHENGSHILI DENTAL MATERIAL FACTORY·Registered Oct 01, 2021 – Oct 31, 2022Cancelled
Registration details
Analysis ID
322e0b5e6a9633ce02888ed6ac182265
Customs Code
DHA08600304300
Company information
Manufacturer Country
China
Authorized Representative
CHANG HSIN BIOTECH CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of occlusal paper (F.6140) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.6140 Occlusal paper
Import Information
Chinese goods;; input
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2022
Cancellation Date
Feb 01, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Changxin Seigi" occlusal paper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 322e0b5e6a9633ce02888ed6ac182265 and manufactured by TIANJIN SHENGSHILI DENTAL MATERIAL FACTORY. The authorized representative in Taiwan is CHANG HSIN BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TIANJIN SHENGSHILI DENTAL MATERIAL FACTORY, 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.

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