Taiwan FDA registration 0a22f7200da565271d06f8689d911054

Aon drainage bottle and connecting sleeve (sterilization)

TW: “怡安”引流瓶及連接管套組 (滅菌)

Taiwan·Risk Class 1·LILY MEDICAL CORPORATION·Registered Mar 10, 2014 – Mar 10, 2019Cancelled

Registration details

Analysis ID: 0a22f7200da565271d06f8689d911054

Company information

Manufacturer: LILY MEDICAL CORPORATION
Manufacturer Country: Taiwan, Province of China
Authorized Representative: LILY MEDICAL CORPORATION

Product details

Intended Use: Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" and "vacuum powered body fluid absorption device (J.6740)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): J General hospital and personal use equipment;; I General, Plastic Surgery and Dermatology
Product Type (Level 2): J.6740 Vacuum powered fluid absorption apparatus;; I.4680 Non-motive, single patient-use, carry-on suctioning device
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: Mar 10, 2014
Expiry Date: Mar 10, 2019
Cancellation Date: May 19, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Aon drainage bottle and connecting sleeve (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0a22f7200da565271d06f8689d911054 and manufactured by LILY MEDICAL CORPORATION. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.

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