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Device Explorer · FDA GUDID · GMDN 46429

Electrical-only medical device connection cable, reprocessed

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).

US‑registered devices413in commercial distribution
Companies8labelers on GUDID
Single‑use84%of device records
Sterile93%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Innovative Health Llc13934%
Stryker Sustainability Solutions, Inc.12230%
Medline Industries, Inc.5814%
Sterilmed, Inc.5012%
Grace Manufacturing, Inc.246%
Irvine Biomedical, Inc.164%
Edan Instruments, Inc.20%
Cortex, Inc.20%

Top labelers

CompanyDevicesShare
Innovative Health Llc13934%
Stryker Sustainability Solutions, Inc.12230%
Medline Industries, Inc.5814%
Sterilmed, Inc.5012%
Grace Manufacturing, Inc.246%
Irvine Biomedical, Inc.164%
Edan Instruments, Inc.20%
Cortex, Inc.20%

Company = labeler of record on GUDID. 8 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

N/AIntellanav Ablation CableBaylis Medical NRGMedtronicConnection CableSJM™NASafire™ TXOptiMap™ System Interconnect CableOptiMap™Catheter Extension CableMEDLINEGreenwald Surgical Company, Inc.Greenwald Surgical Device Company, Inc.

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
IKDCABLE, ELECTRODE142
IKDCable, Electrode136
NLHCATHETER, RECORDING, ELECTRODE, REPROCESSED84
DSACABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECT59
HGIElectrocautery, Gynecologic (And Accessories)14
FBJCord, Electric For Transurethral Surgical Instrument9

GMDN & GCC registration

  • GMDN code 46429 · non‑implantable
  • Single‑use 84% · sterile 93% · Rx‑only 100% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Centimeter) · 88Length (Feet) · 78Length (Meter) · 11

Use these as the dimensions to specify in a tender line.

How many electrical-only medical device connection cable, reprocessed products are registered in the US?

413 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Electrical-only medical device connection cable, reprocessed", from 8 companies. The largest labeler is Innovative Health Llc with 34% of records.

Which FDA product codes apply?

IKD (CABLE, ELECTRODE), IKD (Cable, Electrode), NLH (CATHETER, RECORDING, ELECTRODE, REPROCESSED), DSA (CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECT)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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