Consulting Wallah › Device Explorer › Other devices › Percutaneous radio-frequency ablation probe, tumou
Device Explorer · FDA GUDID · GMDN 64233

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

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 bipolar conf

US‑registered devices155in commercial distribution
Companies6labelers on GUDID
Single‑use99%of device records
Sterile72%labelled sterile
Prescription92%Rx‑only share
ShareLinkedIn

Share of device records

Cambridge Interventional Llc10769%
Merit Medical Systems, Inc.1812%
Stryker Corporation106%
Zhejiang Curaway Medical Technology Co., Ltd.106%
Medtronic Sofamor Danek, Inc.85%
Axon Srl21%

Top labelers

CompanyDevicesShare
Cambridge Interventional Llc10769%
Merit Medical Systems, Inc.1812%
Stryker Corporation106%
Zhejiang Curaway Medical Technology Co., Ltd.106%
Medtronic Sofamor Danek, Inc.85%
Axon Srl21%

Company = labeler of record on GUDID. 6 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

OptaBlateOptablateCurawaySpineSTAR®STAR™SPINERY NeedleProcedureKitCRFElectrodeCRFOsteoCool™ RF Ablation System

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 & Accessories123
GEIElectrosurgical, cutting & coagulation & accessories25
GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES7

GMDN & GCC registration

  • GMDN code 64233 · non‑implantable
  • Single‑use 99% · sterile 72% · Rx‑only 92% · 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 (Millimeter) · 7

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

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

155 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, bipolar", from 6 companies. The largest labeler is Cambridge Interventional Llc with 69% of records.

Which FDA product codes apply?

GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEI (Electrosurgical, cutting & coagulation & accessories), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES)

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.

How do I get quotes?

Add percutaneous radio-frequency ablation probe, tumour-ablation, bipolar to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.

Request quotes for Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar

Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.

Buying percutaneous radio-frequency ablation probe, tumou for a hospital group?Free executive assessment: we benchmark your prices and tender structure against the Network.
Book the free assessment

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.

Get quotes →