Taiwan FDA registration 728aa99e26c74a72483aeb3589ea7498

"Planmeca" Optical Impression Systems for CAD/CAM (Non-Sterile)

TW: "普洛美嘉" CAD/CAM光學取模系統 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·PLANMECA OY·Registered Oct 01, 2021 – Oct 31, 2023Expired
Registration details
Analysis ID
728aa99e26c74a72483aeb3589ea7498
License Form
Ministry of Health Medical Device Import Registration No. 018763
Customs Code
DHA08401876300
Company information
Manufacturer
PLANMECA OY
Manufacturer Country
Finland
Authorized Representative
MIDEAL TECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of CAD/CAM optical mold taking system (F.3661) for the management of medical equipment.
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F3661 CAD/CAM optical mold taking system
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2023
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About this record

Access comprehensive regulatory information for "Planmeca" Optical Impression Systems for CAD/CAM (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 728aa99e26c74a72483aeb3589ea7498 and manufactured by PLANMECA OY. The authorized representative in Taiwan is MIDEAL TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PLANMECA OY, 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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