Taiwan FDA registration f2ebc81e251575ff242ad7ff504c5771
Aon Connection Pipe (Sterilization)
TW: 〝怡安〞連接管 (滅菌)
Registration details
- Analysis ID
- f2ebc81e251575ff242ad7ff504c5771
- Customs Code
- DHA04600153603
Company information
- Manufacturer Country
- China
- Authorized Representative
- LILY MEDICAL CORPORATION
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- Chinese goods;; Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 02, 2011
- Expiry Date
- Dec 02, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Aon Connection Pipe (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f2ebc81e251575ff242ad7ff504c5771 and manufactured by JIANGSU YAOHUA MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.
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