"Tecan" Microplate readers (Non-Sterile)
Taiwan·Risk Class 1·MD·TECAN AUSTRIA GMBH·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 096871e1c9a61035ede82b9c15f27068
- License Form
- Ministry of Health Medical Device Import Registration No. 021365
- Customs Code
- DHA08402136508
- Manufacturer
- TECAN AUSTRIA GMBH
- Manufacturer Country
- Austria
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
- 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)
- A2300 Colorimeter, photometer, or spectrophotometer for clinical use
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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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.