Taiwan FDA registration d680a969f31a81d1b1f6f1053cb0e62c

"J.Morita" Tri Auto ZX2 Dental Handpiece and Accessories (Non-Sterile)

TW: "莫莉塔" 揣歐拓麗可仕2牙科手機及其附件 (未滅菌)

Taiwan·Risk Class 1·MD·J. MORITA MFG. CORP.·Registered Jun 08, 2017 – Jun 08, 2027Active

Registration details

Analysis ID: d680a969f31a81d1b1f6f1053cb0e62c
License Form: Ministry of Health Medical Device Import No. 017940
Customs Code: DHA09401794000

Company information

Manufacturer: J. MORITA MFG. CORP.
Manufacturer Country: Japan
Authorized Representative: PRODENT CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of medical equipment management measures dental handpieces and their accessories (F.4200).
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4200 Dental Handpiece and its accessories
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 08, 2017
Expiry Date: Jun 08, 2027

About this record

Access comprehensive regulatory information for "J.Morita" Tri Auto ZX2 Dental Handpiece 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 d680a969f31a81d1b1f6f1053cb0e62c and manufactured by J. MORITA MFG. CORP.. The authorized representative in Taiwan is PRODENT CO., LTD..

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.