Taiwan FDA registration 8e18a71405727d4e508bd5e0b5fb71eb

"Taica" Manual patient transfer device (Non-Sterile)

TW: "泰已科" 手動病患輸送裝置 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TAICA CORPORATION·Registered Oct 01, 2021 – Oct 31, 2022Cancelled
Registration details
Analysis ID
8e18a71405727d4e508bd5e0b5fb71eb
License Form
Ministry of Health Medical Device Import Registration No. 017396
Customs Code
DHA08401739604
Company information
Manufacturer
TAICA CORPORATION
Manufacturer Country
Japan
Authorized Representative
FUROTO MEDICAL & WELFARE CO., LTD.
Product details
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J6785 Manual Patient Conveyor
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Taica" Manual patient transfer device (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 8e18a71405727d4e508bd5e0b5fb71eb and manufactured by TAICA CORPORATION. The authorized representative in Taiwan is FUROTO MEDICAL & WELFARE CO., LTD..

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