Taiwan FDA registration e21825a83ebf856708672228da347831

"Meionriki" manual osteologic surgical instrument (unsterilized)

TW: "美恩力" 手動式骨科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·CANWELL MEDICAL CO, LTD.·Registered Jan 17, 2019 – Jan 17, 2024Expired
Registration details
Analysis ID
e21825a83ebf856708672228da347831
Customs Code
DHA09600366800
Company information
Manufacturer Country
China
Authorized Representative
MENEY CO., LTD.
Product details
Intended Use
Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.4540 手動式骨科手術器械
Import Information
Chinese goods;; input
Dates and status
Registration Date
Jan 17, 2019
Expiry Date
Jan 17, 2024
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About this record

Access comprehensive regulatory information for "Meionriki" manual osteologic surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e21825a83ebf856708672228da347831 and manufactured by CANWELL MEDICAL CO, LTD.. The authorized representative in Taiwan is MENEY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SAZEENO INDUSTRIES, SUZHOU SUNAN ZIMMERED MEDICAL INSTRUMENT CO., LTD., 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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