Taiwan FDA registration ade09c093de9af8450b9a69ca1f864a0

"Meiku" unilateral artificial knee tibial pad

TW: “美酷”單側人工膝關節脛骨內墊

Taiwan·Risk Class 2·MAKO Surgical Corp.;; HOWMEDICA OSTEONICS CORP.·Registered Feb 23, 2022 – Feb 23, 2027Active

Registration details

Analysis ID: ade09c093de9af8450b9a69ca1f864a0
Customs Code: DHA05603527407

Company information

Manufacturer: MAKO Surgical Corp.;; HOWMEDICA OSTEONICS CORP.
Manufacturer Country: United States
Authorized Representative: STRYKER FAR EAST INC. TAIWAN BRANCH (USA)

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.3520 Non-restrictive femoral tibial metal/polymer cemented remedy for knee joints
Import Information: import

Dates and status

Registration Date: Feb 23, 2022
Expiry Date: Feb 23, 2027

About this record

Access comprehensive regulatory information for "Meiku" unilateral artificial knee tibial pad in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ade09c093de9af8450b9a69ca1f864a0 and manufactured by MAKO Surgical Corp.;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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