Order Entry
United States
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Helix Elite Inactivated Standard, Microbiologics
  76199-858
 :  Avantor
 :  
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Helix Elite Inactivated Standard, Microbiologics
  76199-858
 :  Avantor
 :  
Restricted Products: To process your orders without delay, please provide the required business documentation to purchase this product.

To order chemicals, medical devices, or other restricted products please provide ID that includes your business name & shipping address via email [email protected] or fax 484.881.5997 referencing your VWR account number. Acceptable forms of ID are:

  • • State issued document with your organization's Federal Tax ID Number
  • • State issued document with your organization's Resale Tax ID Number
  • • City or County issued Business License
  • • State Department of Health Services License
  • • Any other ID issued by the State that includes the business name & address

* ATTN: California Customers may require additional documentation as part of the CA Health & Safety Code. Products that fall under this regulation will be placed on a mandatory 21-day hold after documentation is received. Avantor will not lift restrictions for residential shipping addresses.

 

  • Description:
    Inactivated Enterovirus D68
  • Environmentally Preferable:
  • Cat. No.:
    76199-858

 

 

Inactivated Helix Elite Molecular Standards are used for every step of the molecular testing process, from extraction, to amplification and detection.

  • Fully intact, non-viable process controls
  • FDA listed and CE Marked as an In-Vitro Diagnostic (IVD) Medical Device
  • Used for every step of the molecular testing process, from extraction, to amplification and detection
  • Quick dissolving lyophilized pellets may be reconstituted in buffer or transport medium
  • Processed using the same protocols as the patient sample

Inactivated Helix Elite Molecular Standards are used for every step of the molecular testing process, from extraction, to amplification and detection. Quick dissolving lyophilized pellets may be reconstituted in buffer or transport medium. These are FDA listed and CE Marked as an In-Vitro Diagnostic (IVD) Medical Device, processed using the same protocols as the patient sample, and fully intact, non-viable process controls.