Taiwan FDA registration 2924dcc50c133e9028ffb7e480faa425
“Lily” Disposable Spinal Fluid Manometer
TW: “怡安”拋棄式脊髓液壓力計
Taiwan·Risk Class 2·MD·LILY MEDICAL CORPORATION·Registered Jul 17, 2018 – Jul 17, 2028ActiveRegistration details
- Analysis ID
- 2924dcc50c133e9028ffb7e480faa425
- License Form
- Ministry of Health Medical Device Manufacturing No. 006163
Company information
- Manufacturer
- LILY MEDICAL CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LILY MEDICAL CORPORATION
Product details
- Intended Use
- It is suitable for patients who measure cerebrospinal cord hydraulic pressure (C.S.F. Pressure) before and after lumbar puncture sampling or drainage.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J2500 Spinal fluid manometer
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 17, 2018
- Expiry Date
- Jul 17, 2028
About this record
Access comprehensive regulatory information for “Lily” Disposable Spinal Fluid Manometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2924dcc50c133e9028ffb7e480faa425 and manufactured by LILY MEDICAL CORPORATION. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.
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