Taiwan FDA registration f0271b5bd91c257378beeac0064c4edd

"Mitek" Arthroscope Accessories (Non-Sterile)

TW: "邁特" 關節鏡附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DEPUY MITEK, INC.·Registered Aug 27, 2020 – Aug 27, 2025Expired
Registration details
Analysis ID
f0271b5bd91c257378beeac0064c4edd
License Form
Ministry of Health Medical Device Import No. 021903
Customs Code
DHA09402190306
Company information
Manufacturer
DEPUY MITEK, INC.
Manufacturer Country
United States
Authorized Representative
JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
Intended Use
Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
N Orthopedic devices
Product Type (Level 2)
N1100 Arthroscopy
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 27, 2020
Expiry Date
Aug 27, 2025
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About this record

Access comprehensive regulatory information for "Mitek" Arthroscope 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 f0271b5bd91c257378beeac0064c4edd and manufactured by DEPUY MITEK, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDOS INTERNATIONAL SARL, 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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