Pure Global

"Xincheng" alternating decompression air mattress (unsterilized) - Taiwan Registration d831cbfee0ae2cd7cd8b752fee6c9ee9

Access comprehensive regulatory information for "Xincheng" alternating decompression air mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d831cbfee0ae2cd7cd8b752fee6c9ee9 and manufactured by ROODINSEAT CORPORATION. The authorized representative in Taiwan is ROODINSEAT CORPORATION.

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
d831cbfee0ae2cd7cd8b752fee6c9ee9
Registration Details
Taiwan FDA Registration: d831cbfee0ae2cd7cd8b752fee6c9ee9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Xincheng" alternating decompression air mattress (unsterilized)
TW: "้‘ซๆˆ"ไบคๆ›ฟๅผๆธ›ๅฃ“ๆฐฃๅขŠๅบŠ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d831cbfee0ae2cd7cd8b752fee6c9ee9

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".

J General hospital and personal use equipment

J.5550 ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ

Domestic

Dates and Status

Jan 10, 2012

Jan 10, 2022

Apr 12, 2024

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ