Taiwan FDA registration 31e2ee1bb10d8658da4b9ae0769745cc

"Hordeka Osterning" artificial acetabular component system

TW: “好美得卡奧斯得寧”人工髖臼組件系統

Taiwan·Risk Class 2·STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered Dec 18, 2012 – Dec 18, 2027Active

Registration details

Analysis ID: 31e2ee1bb10d8658da4b9ae0769745cc
Customs Code: DHA00602434704

Company information

Manufacturer: STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.
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.3358 Semi-restricted correlated metals/polymers/metals porous coating and cementless cement supplements
Import Information: import

Dates and status

Registration Date: Dec 18, 2012
Expiry Date: Dec 18, 2027

About this record

Access comprehensive regulatory information for "Hordeka Osterning" artificial acetabular component system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 31e2ee1bb10d8658da4b9ae0769745cc 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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