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“Lily” Disposable Spinal Fluid Manometer - Taiwan Registration 2924dcc50c133e9028ffb7e480faa425

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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2924dcc50c133e9028ffb7e480faa425
Registration Details
Taiwan FDA Registration: 2924dcc50c133e9028ffb7e480faa425
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Device Details

“Lily” Disposable Spinal Fluid Manometer
TW: “怡安”拋棄式脊髓液壓力計
Risk Class 2
MD

Registration Details

2924dcc50c133e9028ffb7e480faa425

Ministry of Health Medical Device Manufacturing No. 006163

Company Information

Taiwan, Province of China

Product Details

It is suitable for patients who measure cerebrospinal cord hydraulic pressure (C.S.F. Pressure) before and after lumbar puncture sampling or drainage.

J General hospital and personal use equipment

J2500 Spinal fluid manometer

Produced in Taiwan, China

Dates and Status

Jul 17, 2018

Jul 17, 2028