Taiwan FDA registration a39e7e06e79e6c02f896060d7e21f54a
"Aon" drainage bottle and connecting sleeve (sterilization)
TW: "怡安" 引流瓶及連接管套組 (滅菌)
Registration details
- Analysis ID
- a39e7e06e79e6c02f896060d7e21f54a
Company information
- Manufacturer
- LILY MEDICAL CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LILY MEDICAL CORPORATION
Product details
- Intended Use
- It is limited to the first level of identification scope of "non-powered, single-patient use, portable suction device (I.4680)" in the "Vacuum-powered Body Fluid Absorption Devices (J.6740)" of the Measures for the Classification and Grading 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
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Jun 10, 2015
- Expiry Date
- Jun 10, 2025
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 a39e7e06e79e6c02f896060d7e21f54a and manufactured by LILY MEDICAL CORPORATION. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.
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