Taiwan FDA registration c5cfc44c3309380eafcca8cc64d45402
Shengqing drip rack (unsterilized)
TW: 昇慶點滴架(未滅菌)
Registration details
- Analysis ID
- c5cfc44c3309380eafcca8cc64d45402
- Customs Code
- DHY04300083300
Company information
- Manufacturer
- Shengqing Instrument Factory Co., Ltd
- 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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