Ablation systems
MicroBlate Flex
A non-active, hand-held surgical instrument designed to connect to a microwave ablation system generator to deliver microwaves to a targeted operative site for localized soft-tissue ablation, typically to treat tumours, hydatid cysts and/or menorrhagia. The probe includes a handle and a patient contact region (e.g., antenna, leaflets), and might include a cooling mechanism (via water irrigation). The device is intended to be used in percutaneous, endoscopic [e.g., gastroscopic, laparoscopic], natural orifice or open surgery procedures to ablate tissues (e.g., endometrial ablation). This is a single-use device.
MicroBlate Flex models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 7-AB1-001 | Length 1.00 m; Outer Diameter 2.00 mm | MR Unsafe | Available |
Procedures that use ablation systems
Frequently asked questions
What is MicroBlate Flex used for?
A non-active, hand-held surgical instrument designed to connect to a microwave ablation system generator to deliver microwaves to a targeted operative site for localized soft-tissue ablation, typically to treat tumours, hydatid cysts and/or menorrhagia. The probe includes a handle and a patient contact region (e.g., antenna, leaflets), and might include a cooling mechanism (via water irrigation). The device is intended to be used in percutaneous, endoscopic [e.g., gastroscopic, laparoscopic], natural orifice or open surgery procedures to ablate tissues (e.g., endometrial ablation). This is a single-use device.
Who makes MicroBlate Flex?
MicroBlate Flex is made by Creo Medical Limited. It is listed under tumor ablation systems (microwave, rf, cryo) in our device library.
What sizes does MicroBlate Flex come in?
Sizes listed for MicroBlate Flex: Length: 1 m; Outer Diameter: 2 mm. Confirm availability with the manufacturer's instructions for use.
Is MicroBlate Flex MRI safe?
The FDA device database lists MicroBlate Flex as MR Unsafe. Always follow the specific MRI conditions in the labeling.
Is MicroBlate Flex FDA cleared?
MicroBlate Flex is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Creo Medical Limited sales representative?
Creo Medical Limited has not listed representatives on LA Vascular yet. Visit the Creo Medical Limited company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.