# Venclose Power Cord > Active: European Union and United States. Medical device record on deviCERTS, compiled from public registries. - Canonical page: - Manufacturer: [Venclose, Inc.](https://devicerts.com/manufacturers/venclose-inc) (United States) - Device class: Class I (EU MDR); Class II (US FDA) - FDA product code: GEI - EMDN: Z12010980 ELECTROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES - GMDN: Electrical mains power cable (45804) ## Registrations and authorizations - **EUDAMED** · CE/MDR · European Union · Basic UDI-DI 0858254006VCPCE6G · UDI-DI 00858254006053 · registered 2022-11-12 · status: Active - **GUDID** · GUDID listing · United States · UDI-DI 00858254006053 · listed 2016-11-01 · status: Listed (GUDID: in commercial distribution) - **GUDID** · FDA 510(k) · United States · K160754 · decision 2016-09-09 · decision SESE · status: Active · from GUDID ## Recalls - Z-2638-2025 · Class II · ongoing · initiated 2025-08-21: Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in Venclose EVSRF Ablation Catheters prior to clinical use. This automated diagnostic check is executed immediately upon catheter connection to the generator, occurring before the procedure interface becomes accessible. When a catheter fails this verification process, the generator displays a Red X indicator on the screen without accompanying error codes, effectively disabling catheter functionality. However, BD has determined that software version 3.35 generates false positive failures due to temperature-dependent verification parameters, incorrectly flagging properly functioning Venclose EVSRF Ablation Catheters as defective when the catheter temperature is not at steady state during the check initiation. - Z-0371-2025 · Class II · ongoing · initiated 2024-09-04: The Venclose" RF Ablation Catheters may have been manufactured with internal wiring error. The red and yellow signal wires were soldered on swapped ports of the catheter PCB. This error in wire configuration would lead to power being applied through the proximal 3/4th of the heating coil, bypassing the thermocouple, which will then cause the generator to overdrive the catheter in an attempt to reach desired temperature set point. The wire attachment error causes the device to reach temperatures exceeding the levels intended for therapeutic efficacy, while the console is falsely indicating that temperature has not yet been reached, thus increasing the risk of harm due to excessive temperature. ## Identity - Trade name: Venclose Power Cord [EUDAMED]; Venclose System Power Cord [FDA GUDID (AccessGUDID)] - Generic name: Electrical mains power cable [FDA GUDID (AccessGUDID)] - Model / reference: VC-PC-E [EUDAMED]; VCPCE [FDA GUDID (AccessGUDID)] ## Identifiers - Primary DI / UDI-DI: 00858254006053 [EUDAMED, FDA GUDID (AccessGUDID)] - Basic UDI-DI: 0858254006VCPCE6G [EUDAMED] - 510(k) Number: K160754 [FDA GUDID (AccessGUDID)] - FDA product code: GEI [FDA GUDID (AccessGUDID)] - EMDN code: Z12010980 [EUDAMED] - GMDN term: Electrical mains power cable (45804) [FDA GUDID (AccessGUDID)] ## Classification - Device class: Class I [EUDAMED]; Class II [FDA GUDID (AccessGUDID)] - Regulation number: 878.4400 [FDA GUDID (AccessGUDID)] - EU registration type: Standard device [EUDAMED] - EU market of registration: Germany [EUDAMED] - GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)] ## Properties - Prescription use: Yes [FDA GUDID (AccessGUDID)] - Lot / batch number: 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)] - Serial number: No [FDA GUDID (AccessGUDID)] - Expiration date: No [FDA GUDID (AccessGUDID)] - Manufacturing date: No [FDA GUDID (AccessGUDID)] ## Source and citation - Cite as: Venclose Power Cord, Venclose, Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/venclose-power-cord-vc-pc-e (data as of 2026-11-15). - Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [FDA recalls](https://open.fda.gov/apis/device/recall/) - Registry records last synced: 2026-10-23 - Statuses computed as of: 2026-11-15 - 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/venclose-power-cord-vc-pc-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.