Taiwan FDA registration 5eba8eaff55401384242847545fa6fe5

"Nefermin" Nadal Legionella Lactobacillus Pneumococcus Urine Antigen Rapid Diagnostic Reagent (Unsterilized)

TW: "奈佛明" 納達爾退伍軍人桿菌肺炎鏈球菌尿液抗原快速診斷試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·NAL VON MINDEN GMBH·Registered Sep 05, 2017 – Sep 05, 2022Cancelled
Registration details
Analysis ID
5eba8eaff55401384242847545fa6fe5
Customs Code
DHA09401826901
Company information
Manufacturer Country
Germany
Authorized Representative
RECHI CO., LTD.
Product details
Intended Use
Limited to the management method of medical equipment, Haemophilus serological reagent (C.3300) and streptococcus serum reagent (C.3740) The first level identification range is limited.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3740 鏈球菌屬血清試劑;; C.3300 嗜血桿菌屬血清試劑
Import Information
import
Dates and status
Registration Date
Sep 05, 2017
Expiry Date
Sep 05, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Nefermin" Nadal Legionella Lactobacillus Pneumococcus Urine Antigen Rapid Diagnostic Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5eba8eaff55401384242847545fa6fe5 and manufactured by NAL VON MINDEN GMBH. The authorized representative in Taiwan is RECHI CO., 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