Taiwan FDA registration dc8924bb1f6feb0c9b218b339d67cc3c

"Kangis Mei" hot and cold compress pad (unsterilized)

TW: “康是美”冷熱敷墊 (未滅菌)

Taiwan·Risk Class 1·Laili Enterprises Co., Ltd·Registered May 11, 2012 – May 11, 2017Cancelled

Registration details

Analysis ID: dc8924bb1f6feb0c9b218b339d67cc3c

Company information

Manufacturer: Laili Enterprises Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PRESIDENT DRUGSTORE BUSINESS CORPORATION

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Discardable Hot and Cold Compress Packs for Medical Use (O.5710)".
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.5710 醫療用可丟棄式的冷熱敷包
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: May 11, 2012
Expiry Date: May 11, 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 "Kangis Mei" hot and cold compress pad (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dc8924bb1f6feb0c9b218b339d67cc3c and manufactured by Laili Enterprises Co., Ltd. The authorized representative in Taiwan is PRESIDENT DRUGSTORE BUSINESS CORPORATION.

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