Taiwan FDA registration 514b23f2710188eb42b0fcce6c4f4291

Stryker Manual Orthopedic Instruments (Sterile/Unsterile)

TW: "史賽克" 手動式骨科手術器械 (滅菌/未滅菌)

Taiwan·Risk Class 1·STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered Jun 17, 2013 – Jun 17, 2028Active

Registration details

Analysis ID: 514b23f2710188eb42b0fcce6c4f4291
Customs Code: DHA04401311202

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: Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.4540 手動式骨科手術器械
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Jun 17, 2013
Expiry Date: Jun 17, 2028

About this record

Access comprehensive regulatory information for Stryker Manual Orthopedic Instruments (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 514b23f2710188eb42b0fcce6c4f4291 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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