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"Leishi" physiological recorder - Taiwan Registration bf0ecd4d53f622806a4e664ac28e795f

Access comprehensive regulatory information for "Leishi" physiological recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf0ecd4d53f622806a4e664ac28e795f and manufactured by Kimball Electronics Group LLC- Jasper;; RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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bf0ecd4d53f622806a4e664ac28e795f
Registration Details
Taiwan FDA Registration: bf0ecd4d53f622806a4e664ac28e795f
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Device Details

"Leishi" physiological recorder
TW: โ€œ็ฃŠไป•โ€็”Ÿ็†่จ˜้Œ„ๅ„€
Risk Class 2

Registration Details

bf0ecd4d53f622806a4e664ac28e795f

DHA05603036307

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.2375 Respiratory frequency monitor

import

Dates and Status

Oct 23, 2017

Oct 23, 2027