Taiwan FDA registration a3b27f77d24b382ec5c2033efb4eafa4

Pushen Ruipu Automatic Microdisc Detector (Unsterilized)

TW: 普生銳普自動微量盤偵測儀(未滅菌)
Taiwan flagTaiwan·Risk Class 1·ROBONIK (INDIA) PVT. LTD.·Registered Jun 21, 2013 – Jun 21, 2023Cancelled
Registration details
Analysis ID
a3b27f77d24b382ec5c2033efb4eafa4
Customs Code
DHA04401312508
Company information
Manufacturer Country
India
Authorized Representative
GENERAL BIOLOGICALS CORP.
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Jun 21, 2013
Expiry Date
Jun 21, 2023
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 Pushen Ruipu Automatic Microdisc Detector (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a3b27f77d24b382ec5c2033efb4eafa4 and manufactured by ROBONIK (INDIA) PVT. LTD.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ROBONIK (INDIA) PVT. LTD., 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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