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"Sonygot" fetal monitoring instrument - Taiwan Registration 80874a237e1abea5ddecd45b946ba7e4

Access comprehensive regulatory information for "Sonygot" fetal monitoring instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 80874a237e1abea5ddecd45b946ba7e4 and manufactured by HUNTLEIGH HEALTHCARE LTD., DIAGNOSTIC PRODUCTS DIVISION. The authorized representative in Taiwan is TRUSHINE 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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80874a237e1abea5ddecd45b946ba7e4
Registration Details
Taiwan FDA Registration: 80874a237e1abea5ddecd45b946ba7e4
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Device Details

"Sonygot" fetal monitoring instrument
TW: "็ดขๅฐผๆ ผ็‰น" ่ƒŽๅ…’็›ฃ่ฆ–ๅ„€ๅ™จ
Risk Class 2
Cancelled

Registration Details

80874a237e1abea5ddecd45b946ba7e4

DHA00601288200

Company Information

Product Details

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

l Obstetrics and Gynecology

import

Dates and Status

Nov 02, 2005

Nov 02, 2015

May 10, 2018

Cancellation Information

Logged out

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