Taiwan FDA registration e0d60518bf63be7ad6d32692293ac71e

“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 Oct 21, 2014 – Oct 21, 2019Cancelled
Registration details
Analysis ID
e0d60518bf63be7ad6d32692293ac71e
License Form
Ministry of Health Medical Device Import No. 014590
Customs Code
DHA09401459007
Company information
Manufacturer
DIACOR
Manufacturer Country
United States
Authorized Representative
SSGI TAIWAN CO.
Product details
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
Oct 21, 2014
Expiry Date
Oct 21, 2019
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期未申請展延
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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 e0d60518bf63be7ad6d32692293ac71e 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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