Taiwan FDA registration dc0741b662f9a1e37044619ad99b6c62
"Good Beauty Oka Osdenin" Ekelay Femur Stalk
TW: “好美得卡 奧斯得寧”愛克雷股骨柄
Taiwan·Risk Class 2·Stryker Ireland Limited;; HOWMEDICA OSTEONICS CORP.·Registered Nov 08, 2016 – Nov 08, 2026ActiveRegistration details
- Analysis ID
- dc0741b662f9a1e37044619ad99b6c62
- Customs Code
- DHA05602902003
Company information
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3353 Semi-restricted Segment Joints of Metallic/Ceramic/Polymer-like Bone Cement or Non-Porous Coating Cement-free Cement-type Supplements
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Nov 08, 2016
- Expiry Date
- Nov 08, 2026
About this record
Access comprehensive regulatory information for "Good Beauty Oka Osdenin" Ekelay Femur Stalk in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc0741b662f9a1e37044619ad99b6c62 and manufactured by Stryker Ireland Limited;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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