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"Saebo" Limb orthosis (Non-Sterile) - Taiwan Registration 57e4138198935f7fe1c195eff1e78227

Access comprehensive regulatory information for "Saebo" Limb orthosis (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 57e4138198935f7fe1c195eff1e78227 and manufactured by SAEBO, INC. The authorized representative in Taiwan is UNION MEDICAL INSTRUMENTS, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SAEBO, INC, and 2 recent registrations in the same category. 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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57e4138198935f7fe1c195eff1e78227
Registration Details
Taiwan FDA Registration: 57e4138198935f7fe1c195eff1e78227
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Device Details

"Saebo" Limb orthosis (Non-Sterile)
TW: "ไผธๅฏถ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

57e4138198935f7fe1c195eff1e78227

Ministry of Health Medical Device Import Registration No. 019664

DHA08401966400

Company Information

United States

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023

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