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"Episi" Manual Orthopedic Surgical Instruments (Sterilized) - Taiwan Registration 88f8ab0b1ac54225cf8331b9add714c0

Access comprehensive regulatory information for "Episi" Manual Orthopedic Surgical Instruments (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88f8ab0b1ac54225cf8331b9add714c0 and manufactured by A PLUS BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is A PLUS BIOTECHNOLOGY 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.

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88f8ab0b1ac54225cf8331b9add714c0
Registration Details
Taiwan FDA Registration: 88f8ab0b1ac54225cf8331b9add714c0
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Device Details

"Episi" Manual Orthopedic Surgical Instruments (Sterilized)
TW: "ๆ„›ๆดพๅธ" ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ(ๆป…่Œ)
Risk Class 1

Registration Details

88f8ab0b1ac54225cf8331b9add714c0

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification scope of manual orthopedic surgical instruments (N.4540) in the management measures for the classification and grading of medical devices.

N Orthopedics

N.4540 ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Nov 21, 2024

Nov 21, 2029