Taiwan FDA registration 75a5fabd1e7790e7833f12ff0a74d6e9

"Koos" Manual Orthopedic Surgical Instruments (Unsterilized)

TW: “科歐思" 手動式骨科手術器械 (未滅菌)

Taiwan·Risk Class 1·SHINEO TECHNOLOGY CO., LTD.·Registered Jan 15, 2021 – Jan 15, 2026Expired

Registration details

Analysis ID: 75a5fabd1e7790e7833f12ff0a74d6e9

Company information

Manufacturer: SHINEO TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CRYORTH 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: Domestic;; Contract manufacturing

Dates and status

Registration Date: Jan 15, 2021
Expiry Date: Jan 15, 2026

About this record

Access comprehensive regulatory information for "Koos" Manual Orthopedic Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 75a5fabd1e7790e7833f12ff0a74d6e9 and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is CRYORTH CO., LTD..

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