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"Aikama Giken" Manual osteologic surgical instrument (unsterile) - Taiwan Registration 7d9b467ea249df3b9c1a4d58402ce618

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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7d9b467ea249df3b9c1a4d58402ce618
Registration Details
Taiwan FDA Registration: 7d9b467ea249df3b9c1a4d58402ce618
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Device Details

"Aikama Giken" Manual osteologic surgical instrument (unsterile)
TW: โ€œๅˆ้ŽฐๆŠ€็ ”โ€ ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

7d9b467ea249df3b9c1a4d58402ce618

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.

N Orthopedics

N.4540 ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

Domestic

Dates and Status

Nov 17, 2010

Nov 17, 2025