Taiwan FDA registration 7d9b467ea249df3b9c1a4d58402ce618
"Aikama Giken" Manual osteologic surgical instrument (unsterile)
TW: “合鎰技研” 手動式骨科手術器械(未滅菌)
Taiwan·Risk Class 1·The first factory of Heyi Technology Co., Ltd·Registered Nov 17, 2010 – Nov 17, 2025ExpiredRegistration details
- Analysis ID
- 7d9b467ea249df3b9c1a4d58402ce618
Company information
- Manufacturer
- The first factory of Heyi Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MONTJADE ENGINEERING 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
Dates and status
- Registration Date
- Nov 17, 2010
- Expiry Date
- Nov 17, 2025
About this record
Access comprehensive regulatory information for "Aikama Giken" Manual osteologic surgical instrument (unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7d9b467ea249df3b9c1a4d58402ce618 and manufactured by The first factory of Heyi Technology Co., Ltd. The authorized representative in Taiwan is MONTJADE ENGINEERING CO., LTD..
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