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"Kaini" nasal aspirator (unsterilized) - Taiwan Registration 14402dac7af4afcdb22ae01b461e2e21

Access comprehensive regulatory information for "Kaini" nasal aspirator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 14402dac7af4afcdb22ae01b461e2e21 and manufactured by KAI INDUSTRIES CO., LTD.. The authorized representative in Taiwan is Jintai Industrial 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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14402dac7af4afcdb22ae01b461e2e21
Registration Details
Taiwan FDA Registration: 14402dac7af4afcdb22ae01b461e2e21
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Device Details

"Kaini" nasal aspirator (unsterilized)
TW: โ€œ่ฒๅฐโ€ๅธ้ผปๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

14402dac7af4afcdb22ae01b461e2e21

DHA04400762200

Company Information

Japan

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Lavage Syringe (J.6960)".

J General hospital and personal use equipment

J.6960 Lavage syringe

import

Dates and Status

Apr 06, 2009

Apr 06, 2014

Jan 09, 2017

Cancellation Information

Logged out

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