Taiwan FDA registration 196aa9eb21dd99c39a9df9ecd9dc945c

“Gyrus”Nasopharyngeal catheter(Non-sterile)

TW: “吉洛氏”鼻咽部導管 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·GYRUS MEDICAL GMBH·Registered Oct 09, 2013 – Oct 09, 2018Cancelled
Registration details
Analysis ID
196aa9eb21dd99c39a9df9ecd9dc945c
License Form
Ministry of Health Medical Device Import No. 013487
Customs Code
DHA09401348709
Company information
Manufacturer
GYRUS MEDICAL GMBH
Manufacturer Country
Germany
Authorized Representative
Yuanyou Industrial Co., Ltd
Product details
Product Type (Level 1)
G ENT device
Product Type (Level 2)
G4175 Nasopharyngeal conduit
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 09, 2013
Expiry Date
Oct 09, 2018
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for “Gyrus”Nasopharyngeal catheter(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 196aa9eb21dd99c39a9df9ecd9dc945c and manufactured by GYRUS MEDICAL GMBH. The authorized representative in Taiwan is Yuanyou 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.

Free DatabasePowered by Pure Global AI89,000+ Devices