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"Bishi" Patient Exit Monitor (Unsterilized) - Taiwan Registration 2c0ff1316462baf3f5852ed50849d682

Access comprehensive regulatory information for "Bishi" Patient Exit Monitor (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2c0ff1316462baf3f5852ed50849d682 and manufactured by PERSONAL SAFETY CORPORATION. The authorized representative in Taiwan is Tianqun Medical Enterprise 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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2c0ff1316462baf3f5852ed50849d682
Registration Details
Taiwan FDA Registration: 2c0ff1316462baf3f5852ed50849d682
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Device Details

"Bishi" Patient Exit Monitor (Unsterilized)
TW: โ€œๆฏ”ๆ€ๅธŒโ€ ็—…ๆ‚ฃ้›ขๅบŠ็›ฃ่ฆ–ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2c0ff1316462baf3f5852ed50849d682

DHA04400826007

Company Information

United States

Product Details

Limited to the first level recognition range of the Bedside Patient Monitor (J.2400) of the Measures for the Administration of Medical Equipment.

J General hospital and personal use equipment

J.2400 Bedside Patient Monitor

import

Dates and Status

Oct 30, 2009

Oct 30, 2014

May 28, 2018

Cancellation Information

Logged out

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