Taiwan FDA registration 250fea32e8ab0638c667f3063ddd46f4

"Holmedeka Osterning" full artificial hip module reset system

TW: “好美得卡奧斯得寧”全人工髖關節模組重置系統

Taiwan·Risk Class 2·Stryker Ireland Limited;; Howmedica, Osteonics Corporation·Registered May 29, 2014 – May 29, 2029Active

Registration details

Analysis ID: 250fea32e8ab0638c667f3063ddd46f4
Customs Code: DHA05602618201

Company information

Manufacturer: Stryker Ireland Limited;; Howmedica, Osteonics Corporation
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.3390 Condylar femoral (hemidybula) metallic/polymer-like bone cement or cementless cement-type supplements;; N.3310 Metallic/polymer-like cement-type or cement-free cement supplements for restricted hip joints; 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: May 29, 2014
Expiry Date: May 29, 2029

About this record

Access comprehensive regulatory information for "Holmedeka Osterning" full artificial hip module reset system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 250fea32e8ab0638c667f3063ddd46f4 and manufactured by Stryker Ireland Limited;; Howmedica, Osteonics Corporation. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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