Taiwan FDA registration eab5d0975d6524921366adb5295e986d

"Stryker" manual instruments for general surgery (non-sterilized)

TW: "史賽克" 一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·HOWMEDICA OSTEONICS CORP.·Registered Apr 29, 2024 – Apr 29, 2029Active

Registration details

Analysis ID: eab5d0975d6524921366adb5295e986d
Customs Code: DHA09402346008

Company information

Manufacturer: HOWMEDICA OSTEONICS CORP.
Manufacturer Country: United States
Authorized Representative: Stryker (Far East) Co., Ltd. Taiwan Branch

Product details

Intended Use: It is limited to the first level of identification scope of the "General Surgical Manual Instruments (I.4800)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Apr 29, 2024
Expiry Date: Apr 29, 2029

About this record

Access comprehensive regulatory information for "Stryker" manual instruments for general surgery (non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eab5d0975d6524921366adb5295e986d and manufactured by HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.

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