Interface Cable

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2-RS2-210

by Creo Medical

Identity

Trade Name: Interface Cable EUDAMED
Croma FDA UDI
Generic Name: Electrical-only medical device connection cable, single-use FDA UDI
Device Name: Interface Cable Procedure Pack EUDAMED
A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. Some types may include an electrical isolator to prevent electrical shocks, and/or a cable cover. This is a single-use device. FDA UDI
Model / Reference: 2-RS2-210 EUDAMED
Interface Cable FDA UDI
Description: A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. Some types may include an electrical isolator to prevent electrical shocks, and/or a cable cover. This is a single-use device. FDA UDI

Identifiers

Catalog Number: 7-RS2-210 FDA UDI
Primary DI / UDI-DI: 05060359560070 EUDAMEDFDA UDI
Basic UDI-DI: 506035956InterfaceCaRS26D EUDAMED
510(k) Number: K171983 FDA UDI
FDA Product Code: KNS FDA UDI
EMDN Code: K02010203 ELECTROSURGERY CONNECTION CABLES, SINGLE-USE EUDAMED
GMDN Term: Electrical-only medical device connection cable, single-use FDA UDI

Classification

Device Class: Class I EUDAMED
Class II FDA UDI
Regulation Number: 876.4300 FDA UDI
Market of Registration: Spain EUDAMED
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

EUDAMEDFDA UDI

Reusable

EUDAMED

Contains Latex

EUDAMEDFDA UDI

Reprocessed

EUDAMED

CMR Substance

EUDAMED

Human-derived

EUDAMED

Human Tissues

EUDAMED

Animal Tissues

EUDAMED

Endocrine Disruptor

EUDAMED

Administering Medicine

EUDAMED

Measuring Function

EUDAMED

Incorporates Medicinal Product

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Interface Cable by Creo Medical — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
EUDAMED	European Union	CE/MDR	506035956InterfaceCaRS26D	Class I	Active
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Creo Medical
EUDAMED SRN: GB-MF-000019076
Authorised Representative: Creo Medical, S.L.U. ES-AR-000001355

Sources (2)

EUDAMED 9a927912-3089-4401-819c-9a8a34eff04f 61 fields · synced Jul 23, 2026
FDA UDI bfc7b0ac-9367-4489-927d-d624934f741f 37 fields · synced May 30, 2026