Helpful product information
Instructions for Use
Looking for help on how to use the Rhinostics collection kits? Check below to see if there are specific instructions for your institution or organization. If not, refer to the general instructions for your particular swab type or collection kit.
Instructions for Use
HUCL Instructions
For a step-by-step guide to Harvard Univeristy Clinical Lab's COVID-19 Self-Swab Collection Kit, click below.
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Instructions for Use and Specifications
RH-100001/LV-2D00001/LV-2D1D001/LV-2D1D002
RHINOstic™ Nasal Swab Collection Devices
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PG-100001/PG-100011
Rhinostics Standard Nasal Swab & Collection Device
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Industry Publications
FDA approvals involving our products (click below for link)
Industry Emergency Use Authorizations (EUAs)
Regulatory Information
Class 1 Exempt Medical Device
The RHINOstic™ Nasal Swab Collection Device and the Standard Nasal Swab are registered as Class I Exempt Medical Devices with the Federal Drug Administration (FDA). Each lot of the RHINOstic™ Nasal Swab Collection Device and the Rhinostics Standard Nasal Swab are sterilized with gamma irradiation. A representative sample of each lot is evaluated for bioburden and all testing procedures are established per the definitions in Clinical Laboratory Standards Institute M40-A2.
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Rhinostics is ever growing to suit patients’ and medical professionals’ needs. Check back soon for more regulatory information.
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