Taiwan FDA registration 8323e8ddad00c1e96030ccb988bfaac3

"Crosstex" Dental operative unit and accessories (Non-Sterile)

TW: "克羅斯" 牙科手術裝置及其附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·CROSSTEX INTERNATIONAL·Registered Jan 29, 2019 – Jan 29, 2024Expired
Registration details
Analysis ID
8323e8ddad00c1e96030ccb988bfaac3
License Form
Ministry of Health Medical Device Import No. 020076
Customs Code
DHA09402007605
Company information
Manufacturer Country
United States
Authorized Representative
BIOCARE TECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F6640 Dental Surgical Devices and Their Accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 29, 2019
Expiry Date
Jan 29, 2024
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About this record

Access comprehensive regulatory information for "Crosstex" Dental operative unit and accessories (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 8323e8ddad00c1e96030ccb988bfaac3 and manufactured by CROSSTEX INTERNATIONAL. The authorized representative in Taiwan is BIOCARE TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CROSSTEX INTERNATIONAL, INC, and 2 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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