# Bc+™ 2U026S

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

- Canonical page: <https://devicerts.com/devices/bc-2u026s>
- Manufacturer: [Copan Italia SpA](https://devicerts.com/manufacturers/copan-italia-spa) (FDA registration: Italy)
- Name in the registry: BC+™ 2U026S
- Device class: Class A (EU IVDR); Class I (US FDA)
- FDA product code: KDT
- EMDN: W050301020102 SAMPLES ANALYSES, PLASTIC TUBES WITHOUT ADDITIVES
- GMDN: Evacuated blood collection tube IVD, no additive (47590)

## Registrations and authorizations

- **EUDAMED** · CE/IVDR · European Union · Basic UDI-DI 80533260DD0190AM001C5 · UDI-DI 08053326004537 · registered 2026-05-20 · status: Active
- **GUDID** · GUDID listing · United States · UDI-DI 08053326004537 · listed 2022-12-07 · status: Listed (GUDID: in commercial distribution)

## Recalls

No recall on record.

## Identity

- Trade name: BC+ [EUDAMED]; BC+™ [FDA GUDID (AccessGUDID)]
- Generic name: Evacuated blood collection tube IVD, no additive [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 2U026S [EUDAMED, FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 08053326004537 [EUDAMED]; 18053326004534 [FDA GUDID (AccessGUDID)]
- Basic UDI-DI: 80533260DD0190AM001C5 [EUDAMED]
- FDA product code: KDT [FDA GUDID (AccessGUDID)]
- EMDN code: W050301020102 [EUDAMED]
- GMDN term: Evacuated blood collection tube IVD, no additive (47590) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class A [EUDAMED]; Class I [FDA GUDID (AccessGUDID)]
- Regulation number: 864.3250 [FDA GUDID (AccessGUDID)]
- EU registration type: Standard device [EUDAMED]
- EU market of registration: Italy [EUDAMED]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Supplied sterile: Yes [EUDAMED, FDA GUDID (AccessGUDID)]
- Single use: Yes [FDA GUDID (AccessGUDID)]
- Professional testing: Yes [EUDAMED]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Premarket exempt: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [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]
- Near-patient testing: No [EUDAMED]
- Companion diagnostics: No [EUDAMED]
- IVD instrument: No [EUDAMED]
- New device: No [EUDAMED]
- 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)]
- Serial number: No [FDA GUDID (AccessGUDID)]
- Manufacturing date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Bc+™ 2U026S, Copan Italia SpA. deviCERTS medical device catalogue. https://devicerts.com/devices/bc-2u026s (data as of 2026-11-15).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [EUDAMED](https://ec.europa.eu/tools/eudamed)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/bc-2u026s.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/bc-2u026s
- 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.