Taiwan FDA registration af75b2abe543f285a312978747bc66fa

"Anjie" medicine cup (unsterilized)

TW: "安捷"藥杯(未滅菌)

Taiwan·Risk Class 1·PACK & PROPER CO., LTD.·Registered Feb 01, 2012 – Feb 01, 2017Cancelled

Registration details

Analysis ID: af75b2abe543f285a312978747bc66fa

Company information

Manufacturer: PACK & PROPER CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PACK & PROPER CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Liquid Drug Dispenser (J.6430)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6430 液體藥物給藥器
Import Information: Domestic

Dates and status

Registration Date: Feb 01, 2012
Expiry Date: Feb 01, 2017
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Anjie" medicine cup (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af75b2abe543f285a312978747bc66fa and manufactured by PACK & PROPER CO., LTD.. The authorized representative in Taiwan is PACK & PROPER CO., LTD..

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