# AquaBeam Robotic System AB2000

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

- Canonical page: <https://devicerts.com/devices/aquabeam-robotic-system-ab2000-d-ab2000-e>
- Manufacturer: [PROCEPT BioRobotics Corporation](https://devicerts.com/manufacturers/fda-fei-3027788423) (United States)
- Device class: Class IIb (EU MDR); Class II (US FDA)
- FDA product code: PZP
- EMDN: Z120106 HYDRODISSECTORS
- GMDN: Water jet knife system (45396)

## Registrations and authorizations

- **EUDAMED** · CE/MDR · European Union · Basic UDI-DI 0850055427AB2000DS · UDI-DI 00850055427020 · registered 2026-05-18 · status: Active
- **GUDID** · FDA 510(k) · United States · K241952 · decision 2024-09-30 · decision SESE · status: Active · from GUDID
- **GUDID** · FDA 510(k) · United States · K231024 · decision 2023-08-30 · decision SESE · status: Active · from GUDID
- **GUDID** · GUDID listing · United States · UDI-DI 00850055427020 · listed 2023-08-25 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA De Novo · United States · DEN170024 · decision 2017-12-21 · decision DENG · status: Active · from GUDID

## Recalls

No recall on record.

## Identity

- Trade name: AquaBeam Robotic System [EUDAMED, FDA GUDID (AccessGUDID)]
- Generic name: Water jet knife system [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: AB2000 [EUDAMED, FDA GUDID (AccessGUDID)]; AB2000-D [FDA GUDID (AccessGUDID)]; AB2000-E [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00850055427020 [EUDAMED, FDA GUDID (AccessGUDID)]
- Basic UDI-DI: 0850055427AB2000DS [EUDAMED]
- Direct marketing DI: 00850055427020 [EUDAMED]
- 510(k) Number: K231024 [FDA GUDID (AccessGUDID)]; K241952 [FDA GUDID (AccessGUDID)]
- De Novo Number: DEN170024 [FDA GUDID (AccessGUDID)]
- FDA product code: PZP [FDA GUDID (AccessGUDID)]
- EMDN code: Z120106 [EUDAMED]
- GMDN term: Water jet knife system (45396) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class IIb [EUDAMED]; Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 876.4350 [FDA GUDID (AccessGUDID)]
- System or procedure pack: System which is a device in itself [EUDAMED]
- EU registration type: Standard device [EUDAMED]
- EU market of registration: Netherlands [EUDAMED]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Clinical & Handling

- MRI safety: MR Unsafe [FDA GUDID (AccessGUDID)]

## Properties

- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Serial number: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Sterilise before use: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Single use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Reusable: No [EUDAMED]
- Contains latex: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Reprocessed single-use device: No [EUDAMED]
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No [EUDAMED]
- Incorporates a substance derived from human blood or plasma: No [EUDAMED]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Contains endocrine-disrupting substances: No [EUDAMED]
- Administering medicine: No [EUDAMED]
- Measuring function: No [EUDAMED]
- Incorporates a medicinal substance: 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)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Lot / batch number: No [FDA GUDID (AccessGUDID)]
- Expiration date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: AquaBeam Robotic System AB2000, PROCEPT BioRobotics Corporation. deviCERTS medical device catalogue. https://devicerts.com/devices/aquabeam-robotic-system-ab2000-d-ab2000-e (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [EUDAMED](https://ec.europa.eu/tools/eudamed)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/aquabeam-robotic-system-ab2000-d-ab2000-e.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/aquabeam-robotic-system-ab2000-d-ab2000-e
- 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.