
Pipeline Flex with Shield Technology 2.50 mm x 10 mm | REF PED-250-10
Medtronic Pipeline Flex with Shield Technology flow diverter, 2.50 mm diameter x 10 mm length, REF PED-250-10, for neurovascular intracranial aneurysm procedures.

The Medtronic Pipeline Flex with Shield Technology (REF PED-300-20) is a braided flow diverter embolization device designed for the endovascular treatment of intracranial aneurysms. This 3.00 mm diameter by 20 mm length configuration features a phosphorylcholine (PC) surface treatment engineered to reduce material thrombogenicity while preserving the flow-diverting performance of the established Pipeline platform.
Key Features
- Flow diverter with Shield Technology phosphorylcholine surface modification
- Braided cobalt-chromium and platinum-tungsten wire construction for radiopacity
- Resheathable and repositionable delivery via the Flex delivery system
- Nominal vessel diameter 3.00 mm; nominal device length 20 mm
- Designed for navigation through tortuous neurovascular anatomy
- Intended for use with compatible microcatheter and guidewire (refer to IFU)
Clinical Applications
- Endovascular reconstruction of intracranial aneurysms
- Treatment of wide-necked and large or giant aneurysms per manufacturer indications
- Parent vessel reconstruction in the anterior circulation per labeled indications
- Procedural use under dual antiplatelet therapy protocols per institutional standards
Product Information
Brand: Medtronic
Product Line: Pipeline Flex with Shield Technology
REF / UPN: PED-300-20
Device Diameter: 3.00 mm
Device Length: 20 mm
Category: Neurovascular / Flow Diverter
Sterility: Supplied sterile for single use (refer to IFU)
Storage: Not specified in the located sources
Regulatory Status: Refer to local regulatory labeling and Instructions for Use
Tell us what product you need and share a few details.
We connect your request with the most relevant verified brands.
Relevant supplier options can respond with availability, documentation context, and quote details.
Practical answers for procurement teams reviewing this product page.
Include the exact product family, brand preference, REF/UPN code when available, required quantity, destination country, expected delivery timing and documentation expectations.
Yes. If alternatives are acceptable, mention equivalent brands, compatible models, size ranges and any non-negotiable requirements.
Related products are connected through structured catalog data such as brand, category, product family and country assignment.
No. This page supports sourcing and RFQ organization. Buyers must verify regulatory status, clinical suitability and procurement compliance independently.
Specific codes reduce ambiguity and help supplier teams identify product availability, packaging details and documentation faster.
Yes. The workflow is designed for hospitals, clinics, distributors, wholesalers, importers and procurement departments.
Yes. Products can be connected to multiple countries in the admin panel, and buyers can specify destination details in the RFQ form.
The request is stored with contact and procurement details so the sourcing conversation can be reviewed and followed up clearly.