Taiwan FDA registration a1d4c1ab77716171bd5c0ae291041e4b

"SILIPOS" Prosthetic and Orthotic Accessory (Non-Sterile)

TW: "矽利波斯" 義肢及裝具用附件 (未滅菌)

Taiwan·Risk Class 1·MD·SILIPOS INC.·Registered Dec 16, 2016 – Dec 16, 2026Active

Registration details

Analysis ID: a1d4c1ab77716171bd5c0ae291041e4b
License Form: Ministry of Health Medical Device Import No. 017295
Customs Code: DHA09401729507

Company information

Manufacturer: SILIPOS INC.
Manufacturer Country: United States
Authorized Representative: COMPLUS INTERNATIONAL CORPORATION

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: Dec 16, 2016
Expiry Date: Dec 16, 2026

About this record

Access comprehensive regulatory information for "SILIPOS" Prosthetic and Orthotic Accessory (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 a1d4c1ab77716171bd5c0ae291041e4b and manufactured by SILIPOS INC.. The authorized representative in Taiwan is COMPLUS INTERNATIONAL CORPORATION.

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