Taiwan FDA registration 15f9009ec257e68c82efdbb76bbf8a6a

“DIACOR” Patient Transport Stretcher (Non-Sterile)

TW: “戴蔻” 病人運送推床 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DIACOR·Registered Jul 08, 2020 – Jul 08, 2025Expired
Registration details
Analysis ID
15f9009ec257e68c82efdbb76bbf8a6a
License Form
Ministry of Health Medical Device Import No. 021715
Customs Code
DHA09402171505
Company information
Manufacturer
DIACOR
Manufacturer Country
United States
Authorized Representative
SSGI TAIWAN CO.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Wheeled Stretcher (J.6910)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J6910 Wheeled stretcher
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 08, 2020
Expiry Date
Jul 08, 2025
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About this record

Access comprehensive regulatory information for “DIACOR” Patient Transport Stretcher (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 15f9009ec257e68c82efdbb76bbf8a6a and manufactured by DIACOR. The authorized representative in Taiwan is SSGI TAIWAN CO..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIACOR, 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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