Taiwan FDA registration 86596646872861859e499388cee29170

DIY Liquid Bandage (Non-Sterile)

TW: 液快絆液體絆創膏(未滅菌)

Taiwan·Risk Class 1·MD·GENEJET BIOTECH CO., LTD.·Registered May 24, 2018 – May 24, 2028Active

Registration details

Analysis ID: 86596646872861859e499388cee29170
License Form: Ministry of Health Medical Device Manufacturing No. 007266

Company information

Manufacturer: GENEJET BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PRESIDENT PHARMACEUTICAL CORPORATION

Product details

Intended Use: Limit the first level identification range of liquid bandages (J.5090) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J5090 Liquid bandages
Import Information: Produced in Taiwan, China; Contract manufacturing

Dates and status

Registration Date: May 24, 2018
Expiry Date: May 24, 2028

About this record

Access comprehensive regulatory information for DIY Liquid Bandage (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 86596646872861859e499388cee29170 and manufactured by GENEJET BIOTECH CO., LTD.. The authorized representative in Taiwan is PRESIDENT PHARMACEUTICAL CORPORATION.

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