# Ca CA3871

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

- Canonical page: <https://devicerts.com/devices/ca-ca3871>
- Manufacturer: [Randox Laboratories, Ltd.](https://devicerts.com/manufacturers/randox-laboratories-ltd)
- Device class: IVD General (EU IVDD); Class II (US FDA)
- FDA product code: CJY
- EMDN: W01010303 CALCIUM
- GMDN: Calcium (Ca2+) IVD, reagent (52875)

## Registrations and authorizations

- **EUDAMED** · CE/IVDD · European Union · Basic UDI-DI B-05055273200904 · UDI-DI 05055273200904 · registered 2026-10-28 · status: Active
- **GUDID** · GUDID listing · United States · UDI-DI 05055273200904 · listed 2016-09-16 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K974607 · decision 1998-02-02 · decision SESE · status: Active · from GUDID

## Recalls

- Z-0839-2019 · Class II · terminated · initiated 2018-12-04: Update to the carryover avoidance technical bulletin to introduce additional steps for reagent carryover avoidance with the Calcium assay on RX instruments. Carryover to the Calcium reagent results may result in falsely elevated or decreased results to both patient and QC samples.

## Identity

- Trade name: CALCIUM (Ca) [EUDAMED]; Ca [FDA GUDID (AccessGUDID)]
- Generic name: Calcium (Ca2+) IVD, reagent [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: CA3871 [EUDAMED, FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 05055273200904 [EUDAMED, FDA GUDID (AccessGUDID)]
- Basic UDI-DI: B-05055273200904 [EUDAMED]
- 510(k) Number: K974607 [FDA GUDID (AccessGUDID)]
- FDA product code: CJY [FDA GUDID (AccessGUDID)]
- EMDN code: W01010303 [EUDAMED]
- GMDN term: Calcium (Ca2+) IVD, reagent (52875) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class IVD General [EUDAMED]; Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 862.1145 [FDA GUDID (AccessGUDID)]
- EU registration type: Legacy device (under a directive) [EUDAMED]
- EU market of registration: Northern Ireland [EUDAMED]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- Reagent: Yes [EUDAMED]
- IVD kit: Yes [EUDAMED]
- Professional testing: Yes [EUDAMED]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Convenience kit: Yes [FDA GUDID (AccessGUDID)]
- 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]
- Self-testing: No [EUDAMED]
- Near-patient testing: No [EUDAMED]
- Companion diagnostics: No [EUDAMED]
- IVD instrument: No [EUDAMED]
- Over-the-counter: 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: Ca CA3871, Randox Laboratories, Ltd. deviCERTS medical device catalogue. https://devicerts.com/devices/ca-ca3871 (data as of 2026-11-15).
- 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: 2026-11-07
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/ca-ca3871.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/ca-ca3871
- 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.