Taiwan FDA registration 08e5cc1fd1b4453b492511fa7d07db2a
Elite Expert Fluorescence Analyzer (Unsterilized)
TW: 美艾利爾 揣業駒 專家型螢光分析儀 (未滅菌)
Registration details
- Analysis ID
- 08e5cc1fd1b4453b492511fa7d07db2a
- Customs Code
- DHA04400682608
Company information
- Manufacturer
- ALERE SAN DIEGO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BIO-CHECK LABORATORIES LTD.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Fluorescence Instrument for Clinical Use (A.2560)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2560 Fluorometer for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Jun 24, 2008
- Expiry Date
- Jun 24, 2023
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for Elite Expert Fluorescence Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 08e5cc1fd1b4453b492511fa7d07db2a and manufactured by ALERE SAN DIEGO, INC.. The authorized representative in Taiwan is BIO-CHECK LABORATORIES LTD..
This page provides complete technical specifications, regulatory compliance details. 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+ Devices