Taiwan FDA registration c5cfc44c3309380eafcca8cc64d45402

Shengqing drip rack (unsterilized)

TW: 昇慶點滴架(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Shengqing Instrument Factory Co., Ltd·Registered Dec 16, 2005 – Dec 16, 2025Expired
Registration details
Analysis ID
c5cfc44c3309380eafcca8cc64d45402
Customs Code
DHY04300083300
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Shengqing Instrument Factory Co., Ltd
Product details
Intended Use
It is a fixed or movable shelf for the purpose of fixing injection solutions and syringe attachments.
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.6990 Injection holder
Import Information
Domestic
Dates and status
Registration Date
Dec 16, 2005
Expiry Date
Dec 16, 2025
About this record

Access comprehensive regulatory information for Shengqing drip rack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c5cfc44c3309380eafcca8cc64d45402 and manufactured by Shengqing Instrument Factory Co., Ltd. The authorized representative in Taiwan is Shengqing Instrument Factory Co., Ltd.

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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