Nano4Imaging GmbH

1 product lines across 1 device categories: Guidewires.

From nano4imaging.com, checked October 2026.

Search Nano4Imaging GmbH guidewires

Is this your company? Claim this page to add product descriptions, indications, sizes and your sales reps by territory.

About Nano4Imaging GmbH

Nano4Imaging GmbH hasn't added a company description yet.

Guidewires

Used in: Uterine Artery Embolization (UAE), Peripheral Balloon Angioplasty, Stroke Thrombectomy, Internal Iliac Artery Embolization

ProductSizes (FDA GUDID)ModelsMRI
Emeryglide
EmeryGlide™ is a sterile, disposable guidewire for the introduction and/or placement of diagnostic or interventional devices. EmeryGlide™ is constructed from a high…
Guidewire Diameter: 0.04 in; Guidewire Length: 180 cm1MR Conditional

Sales representatives

Nano4Imaging GmbH has not listed representatives here yet. Contact the company directly:

From nano4imaging.com, checked October 2026.

Outside their markets or no reply? Send us a request.

Work for Nano4Imaging GmbH? Add a rep and the areas they cover:

FDA clearances and approvals

Frequently asked questions

What devices does Nano4Imaging GmbH make?

Nano4Imaging GmbH has 1 product line in our library across 1 device category: Guidewires.

Are Nano4Imaging GmbH devices FDA cleared?

Our library lists FDA clearances and approvals for Nano4Imaging GmbH products. The most recent is EmeryGlide™ (EG18008901) (510(k) K253262, 2026).

How do I contact a Nano4Imaging GmbH sales representative?

Nano4Imaging GmbH has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.

Does LA Vascular sell Nano4Imaging GmbH products?

No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Nano4Imaging GmbH or its representatives to buy.

Where do the Nano4Imaging GmbH 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.

📬 The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you