Taiwan FDA registration 072fa1796b5c0fd39716ef521d0bac48

Relaxation pregnancy test series

TW: 舒位驗孕測試系列
Taiwan flagTaiwan·Risk Class 2·FIRSTEP BIORESEARCH INC.·Registered Apr 03, 2006 – Apr 03, 2011Cancelled
Registration details
Analysis ID
072fa1796b5c0fd39716ef521d0bac48
Customs Code
DHY00500200900
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
FIRSTEP BIORESEARCH INC.
Product details
Intended Use
The immunoqualitative analysis method was used to test the human chorionic gonadotropin HCG in urine, and the preliminary screening was for pregnancy.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1155 Human chorionic gonadotropin testing system
Import Information
Domestic
Dates and status
Registration Date
Apr 03, 2006
Expiry Date
Apr 03, 2011
Cancellation Date
Nov 01, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Relaxation pregnancy test series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 072fa1796b5c0fd39716ef521d0bac48 and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including IND DIAGNOSTIC INC., ARTRON LABORATORIES INC.;; Yishun International Industrial Co., Ltd, and 2 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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