Taiwan FDA registration bce21e07e692b25f2e092fe2dcbfe09b

“SAR” SAREVAC BODY SPLINT (Non-Sterile)

TW: “莎爾” 伊貝克捲式擔架(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SAR PRODUCTS LTD. (SPECIALIST ACCESS & RESCUE PRODUCTS LTD)·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
bce21e07e692b25f2e092fe2dcbfe09b
License Form
Ministry of Health Medical Device Import Registration No. 021624
Customs Code
DHA08402162406
Company information
Manufacturer Country
United Kingdom
Authorized Representative
REPUTATION AND PROSPERITY CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Portable Stretcher (J.6900)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J6900 portable stretcher
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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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