Taiwan FDA registration cf1dff8445e0ed501233599f291d5f04

"Tecan" Microplate readers (Non-Sterile)

TW: "提肯" 微量盤偵測儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TECAN AUSTRIA GMBH·Registered Mar 13, 2020 – Mar 13, 2025Cancelled
Registration details
Analysis ID
cf1dff8445e0ed501233599f291d5f04
License Form
Ministry of Health Medical Device Import No. 021365
Customs Code
DHA09402136504
Company information
Manufacturer
TECAN AUSTRIA GMBH
Manufacturer Country
Austria
Authorized Representative
EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A2300 Colorimeter, photometer, or spectrophotometer for clinical use
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 13, 2020
Expiry Date
Mar 13, 2025
Cancellation information
Status
Logged out
Reason
轉為登錄字號
Companies making similar products

Top companies providing products similar to ""Tecan" Microplate readers (Non-Sterile)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Tecan" Microplate readers (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cf1dff8445e0ed501233599f291d5f04 and manufactured by TECAN AUSTRIA GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TECAN AUSTRIA GMBH, 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations