Taiwan FDA registration 6f2cbcad0977ff45ed93926fa7a14037

"JAS" Rehabilitation Devices and Accessories (Non-Sterile)

TW: "佳士" 復健用裝具及配件 (未滅菌)

Taiwan·Risk Class 1·MD·JOINT ACTIVE SYSTEMS, INC·Registered Mar 30, 2015 – Mar 30, 2025Expired

Registration details

Analysis ID: 6f2cbcad0977ff45ed93926fa7a14037
License Form: Ministry of Health Medical Device Import No. 015059
Customs Code: DHA09401505901

Company information

Manufacturer: JOINT ACTIVE SYSTEMS, INC
Manufacturer Country: United States
Authorized Representative: JIH FENG LUNG ENTERPRISES COMPANY LTD.

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Accessories for Prosthetics and Accessories for Accessories for Appliances (O.3025)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3025 Accessories for prosthetics and accessories
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 30, 2015
Expiry Date: Mar 30, 2025

About this record

Access comprehensive regulatory information for "JAS" Rehabilitation Devices and Accessories (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 6f2cbcad0977ff45ed93926fa7a14037 and manufactured by JOINT ACTIVE SYSTEMS, INC. The authorized representative in Taiwan is JIH FENG LUNG ENTERPRISES COMPANY LTD..

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