Sensonics' Snap & Sniff Eco-Friendly Olfactory Test System

GUDID G051SNSD0

The Sensonics’ S&S-D test is a member of Snap & Sniff® Olfactory Testing System. This test, along with the other members of the Snap & Sniff® family, was developed to provide scientists, clinicians, and others with a standardized, easy-to-use, and reliable means for evaluating the ability of subjects to discriminate odors. Detailed instructions are provided in an accompanying manual to minimize variability in test administration. The test employs the following odorants: phenyl ethyl alcohol; anethole; amyl acetate; and guaiacol. Formulated at iso-intensive levels, the wands are presented in groups of 3 and the subject is asked to choose which of the 3 is different. The presentation pattern is intuitive and easy to follow. The Snap & Sniff® Discrimination Test kit is comprised of 20 smell “wands”. The odor of a given wand is contained within a proprietary odor-emitting cartridge. When the thumb of the operator pushes forward on a slide mechanism, the odorized tip is exposed for sampling and presented to the subject. Releasing the slide retracts the odorized tip back into the wand’s housing. The Snap & Sniff® mechanism results in an easy presentation of an odorant to a subject. Because the odorant tip is presented only briefly, the odor is retained for much longer periods and can be used for testing many more subjects than devices lacking such sophisticated technology. Liquids, per se, are not present in the sniff wands.

Sensonics, Inc.

Olfactory test stick
Primary Device IDG051SNSD0
NIH Device Record Keybad1cf85-2338-4a07-a795-33b35f3ecc21
Commercial Distribution Discontinuation2025-03-11
Commercial Distribution StatusNot in Commercial Distribution
Brand NameSensonics' Snap & Sniff Eco-Friendly Olfactory Test System
Version Model NumberSNSD
Company DUNS107213563
Company NameSensonics, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com
Phone856-547-7702
Emailsales@sensonics.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCG051SNSD0 [Primary]

FDA Product Code

NRKKit, Test, Olfactory

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2025-03-12
Device Publish Date2025-01-29