Consulting Wallah › Device Explorer › Other devices › Pacing/defibrillation lead stylet
Device Explorer · FDA GUDID · GMDN 46717

Pacing/defibrillation lead stylet

A sterile wire, intended to be percutaneously inserted into the coronary venous vasculature to aid in the transvenous placement and/or removal of implantable pacemaker/defibrillator leads; it may in addition be intended to extract an indwelling catheter or oth

US‑registered devices247in commercial distribution
Companies7labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription99%Rx‑only share
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Share of device records

Medtronic, Inc.9237%
Boston Scientific Corporation7430%
St. Jude Medical, Inc.6526%
Spectranetics Corporation114%
Microport Crm Srl31%
Merit Medical Systems, Inc.10%
Cook Vandergrift Inc.10%

Top labelers

CompanyDevicesShare
Medtronic, Inc.9237%
Boston Scientific Corporation7430%
St. Jude Medical, Inc.6526%
Spectranetics Corporation114%
Microport Crm Srl31%
Merit Medical Systems, Inc.10%
Cook Vandergrift Inc.10%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

SJM™MOND™Locator™Liberator®Liberator Beacon TipLLD EZ Lead Locking DeviceLLD E Lead Locking DeviceLLD #3 Lead Locking DeviceLLD #2 Lead Locking DeviceLLD #1 Lead Locking DeviceLLD Accessory KitLead CutterNAN/AVega

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

FDA product codes

CodeNameDevices
DRBSTYLET, CATHETER220
DTBpermanent pacemaker Electrode35
DRBStylet, Catheter22
LWSImplantable cardioverter defibrillator (non-CRT)12
NVZPulse generator, permanent, implantable6
NVNDrug eluting permanent right ventricular (RV) or right atria6

GMDN & GCC registration

  • GMDN code 46717 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 99% · 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) · 217Outer Diameter (Millimeter) · 144Outer Diameter (Inch) · 95

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

No closely related category with 50+ devices.

How many pacing/defibrillation lead stylet products are registered in the US?

247 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Pacing/defibrillation lead stylet", from 7 companies. The largest labeler is Medtronic, Inc. with 37% of records.

Which FDA product codes apply?

DRB (STYLET, CATHETER), DTB (permanent pacemaker Electrode), DRB (Stylet, Catheter), LWS (Implantable cardioverter defibrillator (non-CRT))

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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