Taiwan FDA registration 78bf76c393d66c868e4c71db2cc6d493
"LILY" Suction Bag and Accessories (Non-Sterile)
TW: "怡安"廢液收集袋及其附件(未滅菌)
Taiwan·Risk Class 1·MD·LILY MEDICAL CORPORATION·Registered Mar 12, 2018 – Mar 12, 2028ActiveRegistration details
- Analysis ID
- 78bf76c393d66c868e4c71db2cc6d493
- License Form
- Ministry of Health Medical Device Manufacturing No. 007160
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 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)
- J6740 Vacuum-powered humoral absorption appliance
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 12, 2018
- Expiry Date
- Mar 12, 2028
About this record
Access comprehensive regulatory information for "LILY" Suction Bag and Accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 78bf76c393d66c868e4c71db2cc6d493 and manufactured by LILY MEDICAL CORPORATION. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.
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