Taiwan FDA registration 25e162e93ff3d80ad8c8336a0a75f565

"Arthrex" Orthopedic Manual Surgical Instrument (Sterile/Non-Sterile)

TW: "艾思瑞斯"手動式骨科手術器械(滅菌/未滅菌)

Taiwan·Risk Class 1·MD·ARTHREX INC.·Registered Jan 11, 2017 – Jan 11, 2027Active

Registration details

Analysis ID: 25e162e93ff3d80ad8c8336a0a75f565
License Form: Ministry of Health Medical Device Import No. 017400
Customs Code: DHA09401740004

Company information

Manufacturer: ARTHREX INC.
Manufacturer Country: United States
Authorized Representative: JOINSMART BIOMEDICAL COMPANY LIMITED

Product details

Intended Use: Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N4540 Manual osteologic surgery instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 11, 2017
Expiry Date: Jan 11, 2027

About this record

Access comprehensive regulatory information for "Arthrex" Orthopedic Manual Surgical Instrument (Sterile/Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25e162e93ff3d80ad8c8336a0a75f565 and manufactured by ARTHREX INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

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