# BD MAX™ Cdiff (US) 443418

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

- Canonical page: <https://devicerts.com/devices/bd-max-cdiff-us-443418>
- Manufacturer: [Becton, Dickinson and Company](https://devicerts.com/manufacturers/becton-dickinson-and-company) (United States)
- Device class: Class II (US FDA)
- FDA product code: OZN
- GMDN: Clostridium difficile nucleic acid IVD, kit, nucleic acid technique (NAT) (50836)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00382904434182 · listed 2016-05-19 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K130470 · decision 2013-04-02 · decision SESE · status: Active · from GUDID

## Recalls

- Z-0238-2026 · Class II · ongoing · initiated 2025-09-23: Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
- Z-0590-2025 · Class II · ongoing · initiated 2024-10-31: BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.

## Identity

- Trade name: BD MAX™ Cdiff (US) [FDA GUDID (AccessGUDID)]
- Generic name: Clostridium difficile nucleic acid IVD, kit, nucleic acid technique (NAT) [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 443418 [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00382904434182 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K130470 [FDA GUDID (AccessGUDID)]
- FDA product code: OZN [FDA GUDID (AccessGUDID)]
- GMDN term: Clostridium difficile nucleic acid IVD, kit, nucleic acid technique (NAT) (50836) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 866.3130 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- 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 [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- 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: BD MAX™ Cdiff (US) 443418, Becton, Dickinson and Company. deviCERTS medical device catalogue. https://devicerts.com/devices/bd-max-cdiff-us-443418 (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: 2026-10-26
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/bd-max-cdiff-us-443418.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/bd-max-cdiff-us-443418
- 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.