# i-STAT 05P71-01

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

- Canonical page: <https://devicerts.com/devices/i-stat-05p71-01>
- Manufacturer: [Abbott Point of Care Inc.](https://devicerts.com/manufacturers/abbott-point-of-care-inc) (United States)
- Device class: IVD General (EU IVDD); Class I (US FDA)
- FDA product code: JJY
- EMDN: W010106040201 MULTIPLE PARAMETERS POC CONTROLS
- GMDN: Multiple blood gas/haemoximetry/electrolyte analyte IVD, control (52860)

## Registrations and authorizations

- **EUDAMED** · CE/IVDD · European Union · Basic UDI-DI B-00054749001064 · UDI-DI 00054749001064 · registered 2026-09-01 · status: Active
- **GUDID** · GUDID listing · United States · UDI-DI 00054749001064 · listed 2023-06-23 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K972868 · decision 1997-08-28 · decision SESE · status: Active · from GUDID

## Recalls

- Z-1314-2024 · Class II · ongoing · initiated 2024-01-09: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes which could increase the probability of an incorrect test result or a delayed test result.
- Z-1315-2024 · Class II · ongoing · initiated 2024-01-09: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes which could increase the probability of an incorrect test result or a delayed test result.

## Identity

- Trade name: i-STAT [EUDAMED, FDA GUDID (AccessGUDID)]
- Generic name: Multiple blood gas/haemoximetry/electrolyte analyte IVD, control [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 05P71-01 [EUDAMED, FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00054749001064 [EUDAMED, FDA GUDID (AccessGUDID)]
- Basic UDI-DI: B-00054749001064 [EUDAMED]
- 510(k) Number: K972868 [FDA GUDID (AccessGUDID)]
- FDA product code: JJY [FDA GUDID (AccessGUDID)]
- EMDN code: W010106040201 [EUDAMED]
- GMDN term: Multiple blood gas/haemoximetry/electrolyte analyte IVD, control (52860) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class IVD General [EUDAMED]; Class I [FDA GUDID (AccessGUDID)]
- Regulation number: 862.1660 [FDA GUDID (AccessGUDID)]
- EU registration type: Legacy device (under a directive) [EUDAMED]
- EU market of registration: Germany [EUDAMED]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- Near-patient testing: Yes [EUDAMED]
- Professional testing: Yes [EUDAMED]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Sterilise before use: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Contains substances of microbial origin: No [EUDAMED]
- Reagent: No [EUDAMED]
- IVD kit: No [EUDAMED]
- Self-testing: No [EUDAMED]
- Companion diagnostics: No [EUDAMED]
- IVD instrument: No [EUDAMED]
- New device: No [EUDAMED]
- 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 05P71-01, Abbott Point of Care Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/i-stat-05p71-01 (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- Registry records last synced: 2026-10-24
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/i-stat-05p71-01.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-05p71-01
- 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.