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Ten Respiratory Pathogens Antigen Rapid Test Kit Medical Device CE Approved Class II
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Ten Respiratory Pathogens Antigen Rapid Test Kit Medical Device CE Approved Class II

MOQ: 1 KIT
Delivery Period: 3-4 days
Payment Method: T/T
Supply Capacity: 100000
Details Information
Product Description
Detail Information
Place of Origin
USA
Brand Name
REAGEN
Certification
CE, ISO
Model Number
RNS92110
Manufacturer:
REAGEN INC
Sample Type:
Rapid Test Kit
Country Of Origin:
United States
Type:
Medical Device
Classification:
Class II
Indications For Use:
Diagnosis Of Disease
Product Name:
Ten Respiratory Pathogens Antigen Rapid Test Kit
Application:
Diagnostic Testing
Highlight:

Class II Rapid Test Kit

,

Medical Device Rapid Test Kit

,

CE Approved Rapid Test Kit

Product Description

Product Description:

This kit is used for in vitro qualitative detection of COVID-19, Influenza A virus, Influenza B virus, Respiratory syncytial virus (RSV),
Adenovirus (ADV), M.Pneumoniae (MP), Chlamydia pneumoniae(CP), Parainfluenza virus 1/3 (PIV1/3), Parainfluenza virus 2(PIV2) and
Human Metapneumovirus(HMPV) antigen in human nasal swab samples.
Ten Respiratory Pathogens Antigen Rapid Test Kit Medical Device CE Approved Class II 0

Features:

  • Product Name: Ten Respiratory Pathogens Antigen Rapid Test Kit
  • Sample Type: Rapid Test Kit
  • Type: Medical Device
  • Country of Origin: United States
  • Warranty: 2 Years
  • Features:
    • Quick and accurate antigen test for ten respiratory pathogens
    • Detects Influenza A/B viruses and COVID-19
    • Easy to use and interpret results
    • Compact and portable
    • Can be used in various healthcare settings
 

Technical Parameters:

Test Format Antigen Rapid Test Kit
Availability Online And In-Store
Country of Origin United States
Sample Type Rapid Test Kit
Product Name Ten Respiratory Pathogens Antigen Rapid Test Kit
Classification Class II
Application Diagnostic Testing
Manufacturer REAGEN INC
Type Medical Device
Indications for Use Diagnosis Of Disease, including covid-19 and influence A/B
 
Storage and Stability
1.The test must remain in the sealed pouch until use. DO NOT FREEZE. Keep away from sunlight. Do not use after the expiration date.
2.Once the package of the test card pouch is opened, it must be used within 30 minutes.
3.The LOT and the expiration date were printed on the labeling.
4.Store as packaged in the sealed pouch at temperature (2-30℃).
5.Shelf life of sample diluent after open is 30 days.
Tags: 

Plasma IgG IgM Detection Reagent,  

Serum IgG IgM Detection Reagent,  

IgG IgM Vitro Diagnostic Reagent

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products
PRODUCTS DETAILS
Products

In Vitro Diagnostic Products

Mycotoxin ELISA Kit

Antibiotic Test Kit

Dairy Milk Testing Kit

Algal Toxin Test Kits

Drug Residue Test Kit

Veterinary Residue Test Kit

Lateral Flow Test Kit

Vitamin Test Kit

ELISA Test Instrument

Pesticide Residue Testing Kit

Pollution Test Kit

Estrogen ELISA kit

Food Composition Testing

Test Kit Manufacturing Technology

Trifluralin Antibodies

Smart Wearable Devices
name
  • name
  • name
Ten Respiratory Pathogens Antigen Rapid Test Kit Medical Device CE Approved Class II
MOQ: 1 KIT
Delivery Period: 3-4 days
Payment Method: T/T
Supply Capacity: 100000
Detail Information
Product Description
Detail Information
Place of Origin
USA
Brand Name
REAGEN
Certification
CE, ISO
Model Number
RNS92110
Manufacturer:
REAGEN INC
Sample Type:
Rapid Test Kit
Country Of Origin:
United States
Type:
Medical Device
Classification:
Class II
Indications For Use:
Diagnosis Of Disease
Product Name:
Ten Respiratory Pathogens Antigen Rapid Test Kit
Application:
Diagnostic Testing
Minimum Order Quantity:
1 KIT
Delivery Time:
3-4 days
Payment Terms:
T/T
Supply Ability:
100000
Highlight

Class II Rapid Test Kit

,

Medical Device Rapid Test Kit

,

CE Approved Rapid Test Kit

Product Description

Product Description:

This kit is used for in vitro qualitative detection of COVID-19, Influenza A virus, Influenza B virus, Respiratory syncytial virus (RSV),
Adenovirus (ADV), M.Pneumoniae (MP), Chlamydia pneumoniae(CP), Parainfluenza virus 1/3 (PIV1/3), Parainfluenza virus 2(PIV2) and
Human Metapneumovirus(HMPV) antigen in human nasal swab samples.
Ten Respiratory Pathogens Antigen Rapid Test Kit Medical Device CE Approved Class II 0

Features:

  • Product Name: Ten Respiratory Pathogens Antigen Rapid Test Kit
  • Sample Type: Rapid Test Kit
  • Type: Medical Device
  • Country of Origin: United States
  • Warranty: 2 Years
  • Features:
    • Quick and accurate antigen test for ten respiratory pathogens
    • Detects Influenza A/B viruses and COVID-19
    • Easy to use and interpret results
    • Compact and portable
    • Can be used in various healthcare settings
 

Technical Parameters:

Test Format Antigen Rapid Test Kit
Availability Online And In-Store
Country of Origin United States
Sample Type Rapid Test Kit
Product Name Ten Respiratory Pathogens Antigen Rapid Test Kit
Classification Class II
Application Diagnostic Testing
Manufacturer REAGEN INC
Type Medical Device
Indications for Use Diagnosis Of Disease, including covid-19 and influence A/B
 
Storage and Stability
1.The test must remain in the sealed pouch until use. DO NOT FREEZE. Keep away from sunlight. Do not use after the expiration date.
2.Once the package of the test card pouch is opened, it must be used within 30 minutes.
3.The LOT and the expiration date were printed on the labeling.
4.Store as packaged in the sealed pouch at temperature (2-30℃).
5.Shelf life of sample diluent after open is 30 days.
Tags: 

Plasma IgG IgM Detection Reagent,

Serum IgG IgM Detection Reagent,

IgG IgM Vitro Diagnostic Reagent

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TEL:: 856-727-0250
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