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Device Explorer · FDA GUDID · GMDN 61933

Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar

A semi-flexible, hand-held surgical instrument intended to be percutaneously introduced via a dedicated cannula [under computed tomography (CT), magnetic resonance imaging (MRI), or ultrasound (US) guidance] to deliver radio-frequency current in a monopolar co

US‑registered devices1,006in commercial distribution
Companies9labelers on GUDID
Single‑use100%of device records
Sterile77%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Cambridge Interventional Llc40040%
Rf Medical Co.,Ltd.32132%
Zhejiang Curaway Medical Technology Co., Ltd.17718%
Starmed Co.,Ltd475%
Navilyst Medical, Inc.313%
Boston Scientific Corporation192%
Medtronic Sofamor Danek, Inc.61%
Medical Disposables Corp30%

Top labelers

CompanyDevicesShare
Cambridge Interventional Llc40040%
Rf Medical Co.,Ltd.32132%
Zhejiang Curaway Medical Technology Co., Ltd.17718%
Starmed Co.,Ltd475%
Navilyst Medical, Inc.313%
Boston Scientific Corporation192%
Medtronic Sofamor Danek, Inc.61%
Medical Disposables Corp30%
Angiodynamics, Inc.20%

Company = labeler of record on GUDID. 9 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CurawayProcedureKitCRFElectrodeCRFTempProbeCRFEndoGuidace ESU Button PencilAccurianAngioDynamicsStarBurstHabibUniblateStarBurst TalonVARY-TIPBIG-TIP™JET-TIP®V-TipRFT Electrode

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

FDA product codes

CodeNameDevices
GEIElectrosurgical, Cutting & Coagulation & Accessories948
GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES53
JOSElectrode, Electrosurgical40
GXIPROBE, RADIOFREQUENCY LESION3
GXIProbe, radiofrequency lesion3

GMDN & GCC registration

  • GMDN code 61933 · non‑implantable
  • Single‑use 100% · sterile 77% · 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) · 68Needle Gauge (Gauge) · 39Catheter Length (Centimeter) · 6Catheter Working Length (Millimeter) · 6Length (Millimeter) · 3

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

How many percutaneous radio-frequency ablation probe, tumour-ablation, monopolar products are registered in the US?

1,006 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar", from 9 companies. The largest labeler is Cambridge Interventional Llc with 40% of records.

Which FDA product codes apply?

GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), JOS (Electrode, Electrosurgical), GXI (PROBE, RADIOFREQUENCY LESION)

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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