Pure Global

"Fantis" decompression cushion (unsterilized) - Taiwan Registration 2fe1727ea0b6b9480868517bac642dac

Access comprehensive regulatory information for "Fantis" decompression cushion (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2fe1727ea0b6b9480868517bac642dac and manufactured by CHENG HOUSE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is FANTASY INDUSTRY CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
2fe1727ea0b6b9480868517bac642dac
Registration Details
Taiwan FDA Registration: 2fe1727ea0b6b9480868517bac642dac
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Fantis" decompression cushion (unsterilized)
TW: โ€œ่Šฌ่’‚ๆ€โ€ๆธ›ๅฃ“ๅๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2fe1727ea0b6b9480868517bac642dac

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification scope of the "Floating Cushion (O.3175)" of the Administrative Measures for Medical Devices.

o Physical Medical Sciences

O.3175 Floating cushion

Domestic;; Contract manufacturing

Dates and Status

Apr 27, 2006

Apr 27, 2011

Nov 23, 2012

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ