Taiwan FDA registration a9f80eafa8ce4932ca947b7707a758c3

"Nanotec" Rapid Analysis Reader (Unsterilized)

TW: “奈米鐵克”快速分析判讀儀(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Nano-Ditech Corporation·Registered May 16, 2019 – May 16, 2024Cancelled
Registration details
Analysis ID
a9f80eafa8ce4932ca947b7707a758c3
Customs Code
DHA09402045500
Company information
Manufacturer Country
United States
Authorized Representative
GRAND MARQUIS 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
Input;; QMS/QSD
Dates and status
Registration Date
May 16, 2019
Expiry Date
May 16, 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 "Nanotec" Rapid Analysis Reader (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a9f80eafa8ce4932ca947b7707a758c3 and manufactured by Nano-Ditech Corporation. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Nano-Ditech Corporation, 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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