Taiwan FDA registration 3abab72f08918aa3465a41a7834f3e49

"Kobayashi" Hana neti wash (unsterilized)

TW: “小林”哈那洗鼻器 (未滅菌)

Taiwan·Risk Class 1·KOBAYASHI PHARMACEUTICAL CO., LTD.·Registered Aug 11, 2008 – Aug 11, 2013Cancelled

Registration details

Analysis ID: 3abab72f08918aa3465a41a7834f3e49
Customs Code: DHA04400698604

Company information

Manufacturer: KOBAYASHI PHARMACEUTICAL CO., LTD.
Manufacturer Country: Japan
Authorized Representative: JEN SHENG PHARMACEUTICAL CO., LTD.

Product details

Intended Use: Limited to the scope of first-class medical equipment management method "Ear, nose and throat drug application (G.5220)". Dosage =
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
Import Information: import

Dates and status

Registration Date: Aug 11, 2008
Expiry Date: Aug 11, 2013
Cancellation Date: Apr 24, 2015

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Kobayashi" Hana neti wash (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3abab72f08918aa3465a41a7834f3e49 and manufactured by KOBAYASHI PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is JEN SHENG PHARMACEUTICAL CO., LTD..

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