Coils

Deltamaxx Cerecyte

by Medos International Sàrl

A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.

Contact a rep Compare similar devices

Deltamaxx Cerecyte models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
CDX180312-30Length 12 cm; Length 190 cm MR ConditionalAvailable
CDX180415-30Length 15 cm; Length 190 cm MR ConditionalAvailable
CDX180520-30Length 20 cm; Length 190 cm MR ConditionalAvailable
CDX180625-30Length 25 cm; Length 190 cm MR ConditionalAvailable
CDX180733-30Length 33 cm; Length 190 cm MR ConditionalAvailable
CDX180835-30Length 35 cm; Length 190 cm MR ConditionalAvailable
CDX180935-30Length 35 cm; Length 190 cm MR ConditionalAvailable
CDX181040-30Length 40 cm; Length 190 cm MR ConditionalAvailable
CDX181242-30Length 42 cm; Length 190 cm MR ConditionalAvailable
CDX181445-30Length 45 cm; Length 190 cm MR ConditionalAvailable
CDX181650-30Length 50 cm; Length 190 cm MR ConditionalAvailable
CDX181855-30Length 55 cm; Length 190 cm MR ConditionalAvailable
CDX182060-30Length 60 cm; Length 190 cm MR ConditionalAvailable
CDX182260-30Length 60 cm; Length 190 cm MR ConditionalAvailable
CDX182460-30Length 60 cm; Length 190 cm MR ConditionalAvailable

FDA clearances

  • 510(k) K120274 March 2012

Procedures that use coils

Frequently asked questions

What is Deltamaxx Cerecyte used for?

A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.

Who makes Deltamaxx Cerecyte?

Deltamaxx Cerecyte is made by Medos International Sàrl. It is listed under embolization coils in our device library.

What sizes does Deltamaxx Cerecyte come in?

Sizes listed for Deltamaxx Cerecyte: Length: 12–190 cm. Confirm availability with the manufacturer's instructions for use.

Is Deltamaxx Cerecyte MRI safe?

The FDA device database lists Deltamaxx Cerecyte as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is Deltamaxx Cerecyte FDA cleared?

Deltamaxx Cerecyte is covered by FDA submission K120274.

How do I contact a Medos International Sàrl sales representative?

Medos International Sàrl has not listed representatives on LA Vascular yet. Visit the Medos International Sàrl 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.

📬 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