Taiwan FDA registration 407f671aad979c092af1b6a6a20bfa9a

BD MAX fully automatic meristem detection system

TW: BD MAX 全自動分生檢測系統
Taiwan flagTaiwan·Risk Class 2·BECTON, DICKINSON AND COMPANY·Registered Apr 20, 2021 – Apr 20, 2026Expired
Registration details
Analysis ID
407f671aad979c092af1b6a6a20bfa9a
Customs Code
DHA05603439705
Company information
Manufacturer Country
United States
Product details
Intended Use
BD MAX systems, when used with appropriate extraction panels and reagents, can automatically extract and purify nucleic acids from a variety of sample types. BD MAX systems can also automatically amplify and detect nucleic acid sequences of interest.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2570 Clinical Multi-standard Detection System Instrument
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Apr 20, 2021
Expiry Date
Apr 20, 2026
About this record

Access comprehensive regulatory information for BD MAX fully automatic meristem detection system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 407f671aad979c092af1b6a6a20bfa9a and manufactured by BECTON, DICKINSON AND COMPANY. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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