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"ArjoHuntleigh" Nonpowered flotation therapy mattress (Non-Sterile) - Taiwan Registration 713d735b4b8256f8d26110b31ff0b86b

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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713d735b4b8256f8d26110b31ff0b86b
Registration Details
Taiwan FDA Registration: 713d735b4b8256f8d26110b31ff0b86b
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Device Details

"ArjoHuntleigh" Nonpowered flotation therapy mattress (Non-Sterile)
TW: "ๆดฑไน…ไบจ็‰นๅˆฉ" ้žๅ‹•ๅŠ›ๅผๆฒป็™‚ๅบŠๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

713d735b4b8256f8d26110b31ff0b86b

Ministry of Health Medical Device Import No. 018593

DHA09401859307

Company Information

Product Details

J General hospital and personal use equipment

J5150 Non-powered treatment mattress

Imported from abroad

Dates and Status

Dec 11, 2017

Dec 11, 2022

Cancellation Information

Logged out

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