Taiwan FDA registration cff445728110598fd4da010173ffc5a0

"Taica" Nonpowered flotation therapy mattress (Non-Sterile)

TW: "泰已科" 非動力式治療床墊 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TAICA CORPORATION·Registered Jan 10, 2017 – Jan 10, 2022Cancelled
Registration details
Analysis ID
cff445728110598fd4da010173ffc5a0
License Form
Ministry of Health Medical Device Import No. 017395
Customs Code
DHA09401739501
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)
J5150 Non-powered treatment mattress
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" Nonpowered flotation therapy mattress (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 cff445728110598fd4da010173ffc5a0 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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