Coils

Deltapaq 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.

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Deltapaq Cerecyte models and sizes

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

Model / catalog no.SizeMRIStatus
CDF100152-30Length 2 cm; Length 190 cm MR ConditionalAvailable
CDF100154-30Length 4 cm; Length 190 cm MR ConditionalAvailable
CDF100156-30Length 6 cm; Length 190 cm MR ConditionalAvailable
CDF100202-30Length 2 cm; Length 190 cm MR ConditionalAvailable
CDF100203-30Length 3 cm; Length 190 cm MR ConditionalAvailable
CDF100204-30Length 4 cm; Length 190 cm MR ConditionalAvailable
CDF100206-30Length 6 cm; Length 190 cm MR ConditionalAvailable
CDF100208-30Length 8 cm; Length 190 cm MR ConditionalAvailable
CDF100210-30Length 10 cm; Length 190 cm MR ConditionalAvailable
CDF100250-30Length 10 cm; Length 190 cm MR ConditionalAvailable
CDF100252-30Length 2 cm; Length 190 cm MR ConditionalAvailable
CDF100254-30Length 4 cm; Length 190 cm MR ConditionalAvailable
CDF100256-30Length 6 cm; Length 190 cm MR ConditionalAvailable
CDF100258-30Length 8 cm; Length 190 cm MR ConditionalAvailable
CDF100304-30Length 4 cm; Length 190 cm MR ConditionalAvailable
CDF100306-30Length 6 cm; Length 190 cm MR ConditionalAvailable
CDF100308-30Length 8 cm; Length 190 cm MR ConditionalAvailable
CDF100310-30Length 10 cm; Length 190 cm MR ConditionalAvailable
CDF100406-30Length 6 cm; Length 190 cm MR ConditionalAvailable
CDF100408-30Length 8 cm; Length 190 cm MR ConditionalAvailable
CDF100410-30Length 10 cm; Length 190 cm MR ConditionalAvailable
CDF100510-30Length 10 cm; Length 190 cm MR ConditionalAvailable
CDF100515-30Length 15 cm; Length 190 cm MR ConditionalAvailable
CDF100612-30Length 12 cm; Length 190 cm MR ConditionalAvailable
CDF100616-30Length 16 cm; Length 190 cm MR ConditionalAvailable
CDF100716-30Length 16 cm; Length 190 cm MR ConditionalAvailable
CDF100720-30Length 20 cm; Length 190 cm MR ConditionalAvailable
CDF100820-30Length 20 cm; Length 190 cm MR ConditionalAvailable
CDF100925-30Length 25 cm; Length 190 cm MR ConditionalAvailable
CDF101025-30Length 25 cm; Length 190 cm MR ConditionalAvailable

FDA clearances

  • 510(k) K080437 May 2008

Procedures that use coils

Frequently asked questions

What is Deltapaq 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 Deltapaq Cerecyte?

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

What sizes does Deltapaq Cerecyte come in?

Sizes listed for Deltapaq Cerecyte: Length: 2–190 cm. Confirm availability with the manufacturer's instructions for use.

Is Deltapaq Cerecyte MRI safe?

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

Is Deltapaq Cerecyte FDA cleared?

Deltapaq Cerecyte is covered by FDA submission K080437.

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.

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