
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-275-10) is a braided flow diversion device designed for the endovascular treatment of intracranial aneurysms. This configuration measures 2.75 mm in diameter by 10 mm in length and incorporates a phosphorylcholine (PC) surface modification intended to reduce material thrombogenicity.
Key Features
Braided multi-wire flow diverter construction with cobalt-chromium and platinum-tungsten strands for radiopacity
Shield Technology surface modification (covalently bonded phosphorylcholine) to reduce material thrombogenicity
Flex delivery system enabling resheathing and repositioning prior to final deployment
Compact 2.75 mm x 10 mm sizing suitable for small parent vessels
Designed for delivery through compatible microcatheters
Clinical Applications
Endovascular flow diversion for intracranial aneurysms
Reconstruction of diseased parent artery segments
Treatment of wide-necked or complex aneurysm morphologies
Use in small-caliber intracranial vasculature consistent with the 2.75 mm device diameter
Product Information
Brand: Medtronic
Category: Neurovascular
REF/UPN: PED-275-10
Device Diameter: 2.75 mm
Device Length: 10 mm
Surface Treatment: Phosphorylcholine (Shield Technology)
Delivery System: Pipeline Flex (resheathable)
Sterility: Supplied sterile, single use
Storage Conditions: Not specified in the located sources
Regulatory Status: Refer to manufacturer IFU for region-specific clearances
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.