Consulting Wallah › Device Explorer › Catheters & tubes › Cardiac mapping catheter, percutaneous, reprocesse
Device Explorer · FDA GUDID · GMDN 46359

Cardiac mapping catheter, percutaneous, reprocessed

A sterile, steerable, flexible tube containing multiple electrodes that is introduced percutaneously into the heart chambers in order to transmit electrical impulses for electrophysiological diagnostic examinations, e.g., intracardiac sensing, endocardial reco

US‑registered devices1,309in commercial distribution
Companies4labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Innovative Health Llc52840%
Stryker Sustainability Solutions, Inc.35127%
Sterilmed, Inc.25219%
Medline Industries, Inc.17814%

Top labelers

CompanyDevicesShare
Innovative Health Llc52840%
Stryker Sustainability Solutions, Inc.35127%
Sterilmed, Inc.25219%
Medline Industries, Inc.17814%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Biosense WebsterN/AMEDLINEReprocessed DECANAV EP Catheter, F CurveReprocessed DECANAV EP Catheter, D CurveNA

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

FDA product codes

CodeNameDevices
NLHCATHETER, RECORDING, ELECTRODE, REPROCESSED1,351
NLHCatheter, Recording, Electrode, Reprocessed521
NLHCatheter, recording, electrode, reprocessed180
DSACABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECT63
NLGCatheter, Intracardiac Mapping, High-Density, Reprocessed7
NLGCatheter, intracardiac mapping, high-density, reprocessed4

GMDN & GCC registration

  • GMDN code 46359 · non‑implantable
  • Single‑use 100% · sterile 100% · 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) · 958

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

How many cardiac mapping catheter, percutaneous, reprocessed products are registered in the US?

1,309 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cardiac mapping catheter, percutaneous, reprocessed", from 4 companies. The largest labeler is Innovative Health Llc with 40% of records.

Which FDA product codes apply?

NLH (CATHETER, RECORDING, ELECTRODE, REPROCESSED), NLH (Catheter, Recording, Electrode, Reprocessed), 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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