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"Tecan" Microplate readers (Non-Sterile) - Taiwan Registration 096871e1c9a61035ede82b9c15f27068

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 096871e1c9a61035ede82b9c15f27068 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.

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096871e1c9a61035ede82b9c15f27068
Registration Details
Taiwan FDA Registration: 096871e1c9a61035ede82b9c15f27068
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Device Details

"Tecan" Microplate readers (Non-Sterile)
TW: "ๆ่‚ฏ" ๅพฎ้‡็›คๅตๆธฌๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

096871e1c9a61035ede82b9c15f27068

Ministry of Health Medical Device Import Registration No. 021365

DHA08402136508

Company Information

Austria

Product Details

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.

A Clinical chemistry and clinical toxicology

A2300 Colorimeter, photometer, or spectrophotometer for clinical use

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

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