Taiwan FDA registration a528362f32f045a577ca58230b847afa

“Boditech” AFIAS-6 Analyzer (Non-Sterile)

TW: “巴迪泰” 自動化螢光免疫分析系統(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Boditech Med Inc.·Registered Apr 13, 2021 – Apr 13, 2026Cancelled
Registration details
Analysis ID
a528362f32f045a577ca58230b847afa
License Form
Ministry of Health Medical Device Import No. 022470
Customs Code
DHA09402247006
Company information
Manufacturer
Boditech Med Inc.
Manufacturer Country
Korea, Republic of
Authorized Representative
PROGRESSIVE GROUP INC.
Product details
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A2160 Individual photometric chemistry analyzer for clinical use
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 13, 2021
Expiry Date
Apr 13, 2026
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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Access comprehensive regulatory information for “Boditech” AFIAS-6 Analyzer (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 a528362f32f045a577ca58230b847afa and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is PROGRESSIVE GROUP INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Boditech Med Inc., 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.

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