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
VIEW PRODUCTGW-UF10001/ GW-F100001
Rhinostics GrooveSwab™
VIEW PRODUCTProduct Information Sheets
Additional Downloads
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, the Standard Nasal Swab, and GrooveSwab™ 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 and the GrooveSwab™ with Ethylene Oxide. 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.
More Information Coming Soon
Rhinostics is ever growing to suit patients’ and medical professionals’ needs. Check back soon for more regulatory information.
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