Coils
Micrusphere Cerecyte
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.
Micrusphere Cerecyte models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| CSP100200-30 | Length 2.5 cm; Length 190 cm | MR Conditional | Available |
| CSP100250-30 | Length 3.3 cm; Length 190 cm | MR Conditional | Available |
| CSP100300-30 | Length 5.4 cm; Length 190 cm | MR Conditional | Available |
| CSP100350-30 | Length 6.6 cm; Length 190 cm | MR Conditional | Available |
| CSP100400-30 | Length 7.5 cm; Length 190 cm | MR Conditional | Available |
| CSP100500-30 | Length 9.7 cm; Length 190 cm | MR Conditional | Available |
| CSP100600-30 | Length 11.9 cm; Length 190 cm | MR Conditional | Available |
| CSP100700-30 | Length 13.9 cm; Length 190 cm | MR Conditional | Available |
| CSP100800-30 | Length 16.1 cm; Length 190 cm | MR Conditional | Available |
| CSP100900-30 | Length 18.4 cm; Length 190 cm | MR Conditional | Available |
| CSP101000-30 | Length 20.3 cm; Length 190 cm | MR Conditional | Available |
| CSP180200-30 | Length 2.7 cm; Length 190 cm | MR Conditional | Available |
| CSP180300-30 | Length 5.8 cm; Length 190 cm | MR Conditional | Available |
| CSP180400-30 | Length 7.9 cm; Length 190 cm | MR Conditional | Available |
| CSP180500-30 | Length 10 cm; Length 190 cm | MR Conditional | Available |
| CSP180600-30 | Length 12.2 cm; Length 190 cm | MR Conditional | Available |
| CSP180700-30 | Length 14.3 cm; Length 190 cm | MR Conditional | Available |
| CSP180800-30 | Length 13.6 cm; Length 190 cm | MR Conditional | Available |
| CSP180900-30 | Length 15.3 cm; Length 190 cm | MR Conditional | Available |
| CSP181000-30 | Length 17.1 cm; Length 190 cm | MR Conditional | Available |
| CSP181100-30 | Length 18.9 cm; Length 190 cm | MR Conditional | Available |
| CSP181200-30 | Length 20.7 cm; Length 190 cm | MR Conditional | Available |
| CSP181300-30 | Length 22.6 cm; Length 190 cm | MR Conditional | Available |
| CSP181400-30 | Length 24.3 cm; Length 190 cm | MR Conditional | Available |
| CSP181500-30 | Length 26 cm; Length 190 cm | MR Conditional | Available |
| CSP181600-30 | Length 27.9 cm; Length 190 cm | MR Conditional | Available |
| CSP181700-30 | Length 30 cm; Length 190 cm | MR Conditional | Available |
| CSP181800-30 | Length 30 cm; Length 190 cm | MR Conditional | Available |
FDA clearances
- 510(k) K082739 October 2008
Procedures that use coils
Frequently asked questions
What is Micrusphere 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 Micrusphere Cerecyte?
Micrusphere Cerecyte is made by Medos International Sàrl. It is listed under embolization coils in our device library.
What sizes does Micrusphere Cerecyte come in?
Sizes listed for Micrusphere Cerecyte: Length: 2.5–190 cm. Confirm availability with the manufacturer's instructions for use.
Is Micrusphere Cerecyte MRI safe?
The FDA device database lists Micrusphere Cerecyte as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Micrusphere Cerecyte FDA cleared?
Micrusphere Cerecyte is covered by FDA submission K082739.
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.