Creo Medical Limited
3 product lines across 1 device categories: Ablation systems.
From creomedical.com, checked November 2026.
About Creo Medical Limited
Creo Medical Limited hasn't added a company description yet.
Tumor Ablation Systems (Microwave, RF, Cryo)
Used in: Liver Tumor Ablation (Microwave or Radiofrequency), Kidney Tumor Ablation (Cryoablation or Microwave)
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| CROMA Electrosurgical Generator The CROMA Electrosurgical Generator is a tabletop, non-network connected, mains powered Electrosurgical Unit (ESU). The CROMA Electrosurgical Generator is intended to provide… | — | 1 | Not stated |
| MicroBlate Flex The AB1 instrument, when used with the Creo Medical Electrosurgical System, is intended for use in coagulation (ablation) of soft tissue. Dimensions:… | Length: 1 m; Outer Diameter: 2 mm | 1 | MR Unsafe |
| MicroBlate Fine MicroBlate Fine (NP1) is a single-use, sterile electrosurgical instrument for use with the Creo Medical Electrosurgical system. It enables ablation of potential… | Length: 1.9 m; Outer Diameter: 2.4 mm | 1 | MR Unsafe |
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From creomedical.com, checked November 2026.
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Frequently asked questions
What devices does Creo Medical Limited make?
Creo Medical Limited has 3 product lines in our library across 1 device category: Ablation systems.
How do I contact a Creo Medical Limited sales representative?
Creo Medical Limited has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.
Does LA Vascular sell Creo Medical Limited products?
No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Creo Medical Limited or its representatives to buy.
Where do the Creo Medical Limited product sizes come from?
From the FDA Global Unique Device Identification Database (GUDID). Confirm sizes and availability with the instructions for use or the manufacturer.
Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.