Taiwan FDA registration 713d735b4b8256f8d26110b31ff0b86b

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

TW: "洱久亨特利" 非動力式治療床墊 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ARJOHUNTLEIGH POLSKA SP. ZO. O.·Registered Dec 11, 2017 – Dec 11, 2022Cancelled
Registration details
Analysis ID
713d735b4b8256f8d26110b31ff0b86b
License Form
Ministry of Health Medical Device Import No. 018593
Customs Code
DHA09401859307
Company information
Manufacturer Country
Poland
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
Dec 11, 2017
Expiry Date
Dec 11, 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 "ArjoHuntleigh" 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 713d735b4b8256f8d26110b31ff0b86b and manufactured by ARJOHUNTLEIGH POLSKA SP. ZO. O.. The authorized representative in Taiwan is TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARJOHUNTLEIGH POLSKA SP. ZO. O., and 2 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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