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"Zimmer" Fijian lumbar intervertebral fusion device - Taiwan Registration 4197a346dcb7022357e4c8da3d101e0c

Access comprehensive regulatory information for "Zimmer" Fijian lumbar intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4197a346dcb7022357e4c8da3d101e0c and manufactured by ZIMMER SPINE. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..

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4197a346dcb7022357e4c8da3d101e0c
Registration Details
Taiwan FDA Registration: 4197a346dcb7022357e4c8da3d101e0c
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Device Details

"Zimmer" Fijian lumbar intervertebral fusion device
TW: ๏ผ‚ๆท้‚๏ผ‚ๆ–ๆฟŸ่…ฐๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2

Registration Details

4197a346dcb7022357e4c8da3d101e0c

DHA00601673201

Company Information

France

Product Details

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

N Orthopedics

import

Dates and Status

Jun 23, 2006

Jun 23, 2026