Taiwan FDA registration ef0ceeaafd9e3ce06471bfc25511fc22

Haishiki Nasal Barrier (Bacterium-Killing)

TW: 海敷樂鼻腔阻隔物 (滅菌)

Taiwan·Risk Class 1·Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory·Registered Oct 20, 2015 – Oct 20, 2025Expired

Registration details

Analysis ID: ef0ceeaafd9e3ce06471bfc25511fc22

Company information

Manufacturer: Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory

Product details

Intended Use: It is limited to the first level of identification of the "Nasal Fixation (G.4780)" of the Administrative Measures for the Classification and Classification of Medical Devices.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4780 Nasal fixations
Import Information: Domestic

Dates and status

Registration Date: Oct 20, 2015
Expiry Date: Oct 20, 2025

About this record

Access comprehensive regulatory information for Haishiki Nasal Barrier (Bacterium-Killing) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef0ceeaafd9e3ce06471bfc25511fc22 and manufactured by Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory. The authorized representative in Taiwan is Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory.

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