Taiwan FDA registration a67474b83d918b18ffb9a3757614ad6b
"Agilent" Microtitration Dilution and Dispensing Equipment (Unsterilized)
TW: "安捷倫" 微滴定稀釋及分配器材(未滅菌)
Registration details
- Analysis ID
- a67474b83d918b18ffb9a3757614ad6b
- Customs Code
- DHA09402085302
Company information
- Manufacturer
- Agilent Technologies, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- AGILENT TECHNOLOGIES TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment classification and grading management method microtitration dilution and dispensing equipment (C.2500).
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2500 微滴定稀釋及分配器材
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 12, 2019
- Expiry Date
- Sep 12, 2024
About this record
Access comprehensive regulatory information for "Agilent" Microtitration Dilution and Dispensing Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a67474b83d918b18ffb9a3757614ad6b and manufactured by Agilent Technologies, Inc.. The authorized representative in Taiwan is AGILENT TECHNOLOGIES TAIWAN 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