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"SILIPOS" Prosthetic and Orthotic Accessory (Non-Sterile) - Taiwan Registration a1d4c1ab77716171bd5c0ae291041e4b

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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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a1d4c1ab77716171bd5c0ae291041e4b
Registration Details
Taiwan FDA Registration: a1d4c1ab77716171bd5c0ae291041e4b
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Device Details

"SILIPOS" Prosthetic and Orthotic Accessory (Non-Sterile)
TW: "็Ÿฝๅˆฉๆณขๆ–ฏ" ็พฉ่‚ขๅŠ่ฃๅ…ท็”จ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a1d4c1ab77716171bd5c0ae291041e4b

Ministry of Health Medical Device Import No. 017295

DHA09401729507

Company Information

United States

Product Details

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)".

o Equipment for physical medicine

O3025 Accessories for prosthetics and accessories

Imported from abroad

Dates and Status

Dec 16, 2016

Dec 16, 2026