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Nipro Prestige IQ

Device Name:Prestige IQ
Manufacturer:

Distributer: Trividia Health Inc. (Formerly Nipro/HDI [Home Diagnostics Inc.]), 2400 NW 55th Court, Fort Lauderdale, FL 33309, UNITED STATES.

Sole: Nipro Corporation, 3-9-3 Honjo-Nishi, Kita-Ku, Osaka 531-8510, JAPAN.

Measuring functions:Blood glucose
Primary Client Use:Intended for both professional use and self-measurement
Measurement Site:Finger and general Alternative Site Testing
Measurement Occurrence:Single measurements only
Availability:Discontinued but still available
Description: The Nipro Prestige IQ is a clinically validated blood glucose meter. Measurements are normally taken from the finger but alternative site testing is allowed and it is intended for both professional use and self-measurement. This device has been discontinued by the manufacturer but may be available through certain outlets.
Assessment:

The technology used in the Nipro Prestige IQ, to measure blood glucose, has passed in a clinical validation study, in a general population, according to a recognised standard protocol, as published in a peer-reviewed publication.

Accuracy AssessmentRecommendationBasis
MedavalLegacy approvalOlder clinical validation; older protocol

Validation Publications

Larbig M, Forst T, Mondok A, Forst S, Pfützner A. Investigation on the accuracy of the blood glucose monitoring device Prestige IQ. Diabetes Nutr Metab. 2003 Aug;16(4):257-61. PMID: 14768776.

15197:2001 - Pass General population