Pure Global

Oji nasal aspirator (unsterilized) - Taiwan Registration e659469e634706ff4188955fc2c2a4ff

Access comprehensive regulatory information for Oji 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 e659469e634706ff4188955fc2c2a4ff and manufactured by STI PLASTICS;; NOVARTIS CONSUMER HEALTH SA. The authorized representative in Taiwan is HALEON UK SERVICES LIMITED TAIWAN BRANCH.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
e659469e634706ff4188955fc2c2a4ff
Registration Details
Taiwan FDA Registration: e659469e634706ff4188955fc2c2a4ff
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Oji nasal aspirator (unsterilized)
TW: ๆญๆฒป้ผปๅธ้ผปๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e659469e634706ff4188955fc2c2a4ff

DHA09401387008

Company Information

France;;Switzerland

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

Input;; Contract manufacturing

Dates and Status

Feb 24, 2014

Feb 24, 2019

Jun 07, 2022

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ