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"Peisi" hearing diagnosis system - Taiwan Registration 8ca33dcd56ea6c31cf7192b2a7eb63a6

Access comprehensive regulatory information for "Peisi" hearing diagnosis system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8ca33dcd56ea6c31cf7192b2a7eb63a6 and manufactured by PATH MEDICAL GMBH. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS CO., LTD..

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8ca33dcd56ea6c31cf7192b2a7eb63a6
Registration Details
Taiwan FDA Registration: 8ca33dcd56ea6c31cf7192b2a7eb63a6
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Device Details

"Peisi" hearing diagnosis system
TW: โ€œๆฒ›ๆ€โ€่ฝๅŠ›่จบๆ–ท็ณป็ตฑ
Risk Class 2

Registration Details

8ca33dcd56ea6c31cf7192b2a7eb63a6

DHA05603167801

Company Information

Germany

Product Details

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

K Neuroscience;; G Otolaryngology

G.1050 ่ฝๅŠ›ๆชขๆŸฅ่จˆ;; K.1900 ่ช˜็™ผๅๆ‡‰่ฒๅˆบๆฟ€ๅ™จ

import

Dates and Status

Oct 15, 2018

Oct 15, 2028