Taiwan FDA registration 17887f9ea848e3785501fb40ccff9a14

Qizhe Color Analyzer (Unsterilized)

TW: 啟哲呈色分析儀(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Kaiwu Technology Co., Ltd. Nanke Factory·Registered Feb 22, 2019 – Feb 22, 2024Cancelled
Registration details
Analysis ID
17887f9ea848e3785501fb40ccff9a14
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Qizhe Biotechnology Co., Ltd
Product details
Intended Use
Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
Import Information
國產;; 委託製造;; QMS/QSD
Dates and status
Registration Date
Feb 22, 2019
Expiry Date
Feb 22, 2024
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for Qizhe Color Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 17887f9ea848e3785501fb40ccff9a14 and manufactured by Kaiwu Technology Co., Ltd. Nanke Factory. The authorized representative in Taiwan is Qizhe Biotechnology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Kaiwu Technology Co., Ltd. Nanke Factory, and 1 recent registrations in the same category. 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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