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"S & F" Robo splint (Non-Sterile) - Taiwan Registration af1f4e6fe79384d28c832df0e01f8b3a

Access comprehensive regulatory information for "S & F" Robo splint (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 af1f4e6fe79384d28c832df0e01f8b3a and manufactured by S&F INC.. The authorized representative in Taiwan is DURAMED 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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af1f4e6fe79384d28c832df0e01f8b3a
Registration Details
Taiwan FDA Registration: af1f4e6fe79384d28c832df0e01f8b3a
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Device Details

"S & F" Robo splint (Non-Sterile)
TW: "่‰พๆ–ฏๆฉๅฏŒ" ่‹ฅ็Žปๆจน่„‚็Ÿณ่†ๅ›บๅฎšๆฟ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

af1f4e6fe79384d28c832df0e01f8b3a

Ministry of Health Medical Device Import Registration No. 002387

DHA08400238701

Company Information

Korea, Republic of

Product Details

Limb equipment is a medical device worn on the upper or lower limbs to support, correct or prevent deformation, and to straighten the body structure for functional improvement.

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026