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"Vansel" Pneumonia Main Pathogen Test Kit (Unsterilized) - Taiwan Registration 575797b164b33229672071ed4e114d91

Access comprehensive regulatory information for "Vansel" Pneumonia Main Pathogen Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 575797b164b33229672071ed4e114d91 and manufactured by VIRCELL, S.L. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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.

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575797b164b33229672071ed4e114d91
Registration Details
Taiwan FDA Registration: 575797b164b33229672071ed4e114d91
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Device Details

"Vansel" Pneumonia Main Pathogen Test Kit (Unsterilized)
TW: "ๅ‡ก่ณฝ็ˆพ" ่‚บ็‚Žไธป่ฆ็—…ๅŽŸๆชขๆธฌๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

575797b164b33229672071ed4e114d91

DHA09401749209

Company Information

Spain

Product Details

Measures for the Administration of Medical Devices "Adenovirus Serum Reagent (C.3020)", "Chlamydomydia Serum Reagent (C.3120)", "Haemophilus Serum Reagent (C.3300)", "Influenzae Virus Serum Reagent (C.3330)", "Mycoplasma Serum Reagent (C.3375)", "Parainfluenza Virus Serum Reagent (C.3400)", "Respiratory Fusion Cell Virus Serum Reagent (C.3480)", "Rickettsial Serum Reagent ( C.3500) first level identification range.

C Immunology and microbiology

C.3300 ๅ—œ่ก€ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘;; C.3375 ้ปดๆผฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘;; C.3120 ๆŠซ่กฃ่Œ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Feb 14, 2017

Feb 14, 2022

Apr 12, 2024

Cancellation Information

Logged out

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