Taiwan FDA registration 7d43f6828c9a1a8bf585d43a6e3c213e

"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 Jan 10, 2017 – Jan 10, 2022Cancelled
Registration details
Analysis ID
7d43f6828c9a1a8bf585d43a6e3c213e
License Form
Ministry of Health Medical Device Import No. 017396
Customs Code
DHA09401739600
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
Jan 10, 2017
Expiry Date
Jan 10, 2022
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 7d43f6828c9a1a8bf585d43a6e3c213e 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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