Taiwan FDA registration 101aebf8a80d87e922040f1f64d2006a

"Difu" artificial knee tibial disc

TW: “帝富”人工膝關節脛骨盤

Taiwan·Risk Class 2·DePuy (Ireland);;DEPUY ORTHOPAEDICS, INC.·Registered Oct 27, 2011 – Oct 27, 2026Active

Registration details

Analysis ID: 101aebf8a80d87e922040f1f64d2006a
Customs Code: DHA00602297602

Company information

Manufacturer: DePuy (Ireland);;DEPUY ORTHOPAEDICS, INC.
Manufacturer Country: Ireland;;United States
Authorized Representative: JOHNSON & JOHNSON MEDICAL TAIWAN LTD.

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.3560 Semi-restrictive knee joints of the femoral bone polymers/metallics/polymers
Import Information: import

Dates and status

Registration Date: Oct 27, 2011
Expiry Date: Oct 27, 2026

About this record

Access comprehensive regulatory information for "Difu" artificial knee tibial disc in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 101aebf8a80d87e922040f1f64d2006a and manufactured by DePuy (Ireland);;DEPUY ORTHOPAEDICS, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

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