Taiwan FDA registration c3b6ff73dee075aa8488591021403627
"Hewang" manual osteologic surgical instrument (sterile)
TW: "喜旺" 手動式骨科手術器械 (滅菌)
Taiwan·Risk Class 1·SEAWON MEDITECH CO., LTD.·Registered Jul 20, 2017 – Jul 20, 2022CancelledRegistration details
- Analysis ID
- c3b6ff73dee075aa8488591021403627
- Customs Code
- DHA09401809402
Company information
- Manufacturer
- SEAWON MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- KROMAX INTERNATIONAL CORP.
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 Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jul 20, 2017
- Expiry Date
- Jul 20, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hewang" manual osteologic surgical instrument (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c3b6ff73dee075aa8488591021403627 and manufactured by SEAWON MEDITECH CO., LTD.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..
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