Taiwan FDA registration fe98517092bf54ddeb8f16ba0b1748bd
Kabang Microtitration Dilution and Dispensing Equipment (Unsterilized)
TW: 卡邦 微滴定稀釋及分配器材 (未滅菌)
Taiwan·Risk Class 1·COPAN WASP S.R.L.·Registered Feb 05, 2020 – Feb 05, 2030ActiveRegistration details
- Analysis ID
- fe98517092bf54ddeb8f16ba0b1748bd
- Customs Code
- DHA09402122807
Company information
- Manufacturer
- COPAN WASP S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- PAN ASIA BIOMEDICAL TECHNOLOGY INC.
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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Feb 05, 2020
- Expiry Date
- Feb 05, 2030
About this record
Access comprehensive regulatory information for Kabang 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 fe98517092bf54ddeb8f16ba0b1748bd and manufactured by COPAN WASP S.R.L.. The authorized representative in Taiwan is PAN ASIA BIOMEDICAL TECHNOLOGY INC..
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