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“SAR” SAREVAC BODY SPLINT (Non-Sterile) - Taiwan Registration bce21e07e692b25f2e092fe2dcbfe09b

Access comprehensive regulatory information for “SAR” SAREVAC BODY 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 bce21e07e692b25f2e092fe2dcbfe09b and manufactured by SAR PRODUCTS LTD. (SPECIALIST ACCESS & RESCUE PRODUCTS LTD). The authorized representative in Taiwan is REPUTATION AND PROSPERITY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SAR PRODUCTS LTD. (SPECIALIST ACCESS & RESCUE PRODUCTS LTD), and 1 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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bce21e07e692b25f2e092fe2dcbfe09b
Registration Details
Taiwan FDA Registration: bce21e07e692b25f2e092fe2dcbfe09b
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Device Details

“SAR” SAREVAC BODY SPLINT (Non-Sterile)
TW: “莎爾” 伊貝克捲式擔架(未滅菌)
Risk Class 1
MD

Registration Details

bce21e07e692b25f2e092fe2dcbfe09b

Ministry of Health Medical Device Import Registration No. 021624

DHA08402162406

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Portable Stretcher (J.6900)".

J General hospital and personal use equipment

J6900 portable stretcher

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

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