# i-STAT 09P31-25

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/i-stat-09p31-25>
- Manufacturer: [Abbott Point of Care Inc.](https://devicerts.com/manufacturers/abbott-point-of-care-inc) (United States)
- Device class: Class II (US FDA)
- FDA product code: JGS
- GMDN: Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent (52861)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 10054749001917 · listed 2016-09-09 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K053110 · decision 2006-01-13 · decision SESE · status: Active · from GUDID

## Recalls

- Z-1846-2025 · Class II · ongoing · initiated 2025-04-24 · matched through shared submission K053110, may concern other models: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
- Z-2022-2011 ·  · terminated · initiated 2011-02-15: i-STAT CHEM 8+ cartridge may generate false results for sodium, chloride and hematocrit.
- Z-1791-2010 ·  · terminated · initiated 2010-02-05 · matched through shared submission K053110, may concern other models: Abbott has determined that there is a dependence of the i-STAT Hct assay on the vertical pitch angle of the i-STAT Analyzer during the blood analysis cycle.

## Identity

- Trade name: i-STAT [FDA GUDID (AccessGUDID)]
- Generic name: Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 09P31-25 [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 10054749001917 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K053110 [FDA GUDID (AccessGUDID)]
- FDA product code: JGS [FDA GUDID (AccessGUDID)]
- GMDN term: Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent (52861) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 862.1665 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Prescription use: No [FDA GUDID (AccessGUDID)]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Serial number: No [FDA GUDID (AccessGUDID)]
- Manufacturing date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: i-STAT 09P31-25, Abbott Point of Care Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/i-stat-09p31-25 (data as of 2026-11-15).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/i-stat-09p31-25.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/i-stat-09p31-25
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.