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“OSMD” Polyether Ether Ketone Interbody Fusion Cage - Taiwan Registration 0c09f802888ae88c55e516ec1d682f6d

Access comprehensive regulatory information for “OSMD” Polyether Ether Ketone Interbody Fusion Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c09f802888ae88c55e516ec1d682f6d and manufactured by OSTEOSTANDARD MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is OSTEOSTANDARD MEDICAL DEVICE CO., LTD..

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0c09f802888ae88c55e516ec1d682f6d
Registration Details
Taiwan FDA Registration: 0c09f802888ae88c55e516ec1d682f6d
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Device Details

“OSMD” Polyether Ether Ketone Interbody Fusion Cage
TW: “沃思坦”聚醚醚酮椎間融合器
Risk Class 2
MD

Registration Details

0c09f802888ae88c55e516ec1d682f6d

Ministry of Health Medical Device Manufacturing No. 006522

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Produced in Taiwan, China

Dates and Status

Aug 18, 2019

Aug 18, 2024