Taiwan FDA registration d977a78fd14cd618697ec72fe0f43511

“Geonic” NASAL ASPIRATOR (Non-Sterile)

TW: "潔恩" 電動吸鼻器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·GEON CORPORATION·Registered Jan 09, 2018 – Jan 09, 2028Active
Registration details
Analysis ID
d977a78fd14cd618697ec72fe0f43511
License Form
Ministry of Health Medical Device Manufacturing No. 007075
Company information
Manufacturer
GEON CORPORATION
Manufacturer Country
Taiwan, Province of China
Authorized Representative
GEON CORPORATION
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Power Nasal Irrigator (G.5550)".
Product Type (Level 1)
G ENT device
Product Type (Level 2)
G5550 powered nose irrigator
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Jan 09, 2018
Expiry Date
Jan 09, 2028
About this record

Access comprehensive regulatory information for “Geonic” NASAL ASPIRATOR (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d977a78fd14cd618697ec72fe0f43511 and manufactured by GEON CORPORATION. The authorized representative in Taiwan is GEON CORPORATION.

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 DatabasePowered by Pure Global AI89,000+ Devices