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"Peisi" multi-function induction hearing examiner - Taiwan Registration d702b63a81f7ae7ebf2886db3bd184b3

Access comprehensive regulatory information for "Peisi" multi-function induction hearing examiner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d702b63a81f7ae7ebf2886db3bd184b3 and manufactured by PATH MEDICAL GMBH. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS 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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d702b63a81f7ae7ebf2886db3bd184b3
Registration Details
Taiwan FDA Registration: d702b63a81f7ae7ebf2886db3bd184b3
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Device Details

"Peisi" multi-function induction hearing examiner
TW: โ€œๆฒ›ๆ€โ€ๅคšๅŠŸ่ƒฝ่ช˜็™ผ่ฝๅŠ›ๆชขๆŸฅๅ„€
Risk Class 2

Registration Details

d702b63a81f7ae7ebf2886db3bd184b3

DHA05603159102

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

Sep 05, 2018

Sep 05, 2028