# Interface Cable Procedure Pack

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

- Canonical page: <https://devicerts.com/devices/interface-cable-procedure-pack-7-rs2-210>
- Manufacturer: [Creo Medical](https://devicerts.com/manufacturers/creo-medical) (United Kingdom)
- Device class: Class I (EU MDR); Class II (US FDA)
- FDA product code: KNS
- EMDN: K02010203 ELECTROSURGERY CONNECTION CABLES, SINGLE-USE
- GMDN: Electrical-only medical device connection cable, single-use (47143)

## Registrations and authorizations

- **EUDAMED** · CE/MDR · European Union · Basic UDI-DI 506035956InterfaceCaRS26D · UDI-DI 05060359560063 · registered 2024-12-10 · status: Active
- **GUDID** · GUDID listing · United States · UDI-DI 05060359560063 · listed 2018-11-15 · status: Listed (GUDID: not in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K171983 · decision 2017-08-17 · decision SESE · status: Active · from GUDID

## Recalls

No recall on record.

## Identity

- Trade name: Interface Cable Procedure Pack [EUDAMED]; Procedure Pack Interface Cable, single use, 1.5 m [FDA GUDID (AccessGUDID)]
- Generic name: Electrical-only medical device connection cable, single-use [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 7-RS2-210 [EUDAMED, FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 05060359560063 [EUDAMED, FDA GUDID (AccessGUDID)]
- Basic UDI-DI: 506035956InterfaceCaRS26D [EUDAMED]
- 510(k) Number: K171983 [FDA GUDID (AccessGUDID)]
- FDA product code: KNS [FDA GUDID (AccessGUDID)]
- EMDN code: K02010203 [EUDAMED]
- GMDN term: Electrical-only medical device connection cable, single-use (47143) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class I [EUDAMED]; Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 876.4300 [FDA GUDID (AccessGUDID)]
- System or procedure pack: Procedure pack which is a device in itself [EUDAMED]
- EU registration type: Standard device [EUDAMED]
- EU market of registration: Northern Ireland [EUDAMED]
- GUDID distribution status: Not in Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- Prescription use: 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 [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)]
- Manufacturing date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Interface Cable Procedure Pack, Creo Medical. deviCERTS medical device catalogue. https://devicerts.com/devices/interface-cable-procedure-pack-7-rs2-210 (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/interface-cable-procedure-pack-7-rs2-210.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/interface-cable-procedure-pack-7-rs2-210
- 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.