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"Pine" alternating decompression air bed (unsterilized) - Taiwan Registration 129b06fdd2c810d3e86b4137b71b31ee

Access comprehensive regulatory information for "Pine" alternating decompression air bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 129b06fdd2c810d3e86b4137b71b31ee and manufactured by Pine Cypress Medical Instrument Co., Ltd. The authorized representative in Taiwan is Pine Cypress Medical Instrument 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.

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129b06fdd2c810d3e86b4137b71b31ee
Registration Details
Taiwan FDA Registration: 129b06fdd2c810d3e86b4137b71b31ee
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Device Details

"Pine" alternating decompression air bed (unsterilized)
TW: โ€œๆพๆŸโ€ไบคๆ›ฟๅผๆธ›ๅฃ“ๆฐฃๅขŠๅบŠ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

129b06fdd2c810d3e86b4137b71b31ee

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

Dec 06, 2007

Dec 06, 2012

Apr 30, 2014

Cancellation Information

Logged out

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