Taiwan FDA registration 5c6d4865b6be638a2e31a87866cf0dd9

"Zeman" extracorporeal shock wave therapy instrument

TW: “采曼”體外震波治療儀

Taiwan·Risk Class 3·Zimmer MedizinSysteme GmbH; Remed Co., Ltd.·Registered Aug 21, 2024 – Aug 21, 2029Active

Registration details

Analysis ID: 5c6d4865b6be638a2e31a87866cf0dd9
Customs Code: DHA05603737500

Company information

Manufacturer: Zimmer MedizinSysteme GmbH; Remed Co., Ltd.
Manufacturer Country: Korea, Republic of;;Germany
Authorized Representative: EASTECH CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.0001 骨科用體外震波系統
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Aug 21, 2024
Expiry Date: Aug 21, 2029

About this record

Access comprehensive regulatory information for "Zeman" extracorporeal shock wave therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5c6d4865b6be638a2e31a87866cf0dd9 and manufactured by Zimmer MedizinSysteme GmbH; Remed Co., Ltd.. The authorized representative in Taiwan is EASTECH CO., LTD..

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