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"Aikman" modular hand bone fusion system - Taiwan Registration 16085b2403c1387dc4955084ab4f5435

Access comprehensive regulatory information for "Aikman" modular hand bone fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16085b2403c1387dc4955084ab4f5435 and manufactured by ACUMED LLC.. The authorized representative in Taiwan is WONDERLAND CORPORATION.

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16085b2403c1387dc4955084ab4f5435
Registration Details
Taiwan FDA Registration: 16085b2403c1387dc4955084ab4f5435
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Device Details

"Aikman" modular hand bone fusion system
TW: โ€œ่‰พๅ…‹ๆ›ผโ€ๆจก็ต„ๅŒ–ๆ‰‹้ชจ่žๅˆ็ณป็ตฑ
Risk Class 2

Registration Details

16085b2403c1387dc4955084ab4f5435

DHA00602043000

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.3030 Single or multiple metallic bone fixation devices and accessories

import

Dates and Status

Nov 24, 2009

Nov 24, 2029