Taiwan FDA registration 6d94075358867be18996135f671bf040

"Meistec" orthopedic manual surgical instrument (Non-Sterile)

TW: "美斯泰克" 手動式骨科手術器械 (未滅菌)

Taiwan·Risk Class 1·MD·MEISTEC CO., LTD.·Registered Apr 21, 2021 – Apr 21, 2026Expired

Registration details

Analysis ID: 6d94075358867be18996135f671bf040
License Form: Ministry of Health Medical Device Import No. 022505
Customs Code: DHA09402250502

Company information

Manufacturer: MEISTEC CO., LTD.
Manufacturer Country: Japan
Authorized Representative: IN ORDER CO., LTD.

Product details

Intended Use: Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N4540 Manual osteologic surgery instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 21, 2021
Expiry Date: Apr 21, 2026

About this record

Access comprehensive regulatory information for "Meistec" orthopedic manual surgical instrument (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 6d94075358867be18996135f671bf040 and manufactured by MEISTEC CO., LTD.. The authorized representative in Taiwan is IN ORDER 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.