Identity
- Trade Name
- DELTAPAQ CERECYTE FDA UDI
- Generic Name
- Neurovascular embolization coil FDA UDI
- Device Name
- DELTAPAQ microcoil DELTAPAQ 10 CERECYTE Coil 6mm x 16cm 190cm Contents: 1 Detachable Coil System FDA UDI
- Model / Reference
- CDF100616-30 FDA UDI
- Description
- DELTAPAQ microcoil DELTAPAQ 10 CERECYTE Coil 6mm x 16cm 190cm Contents: 1 Detachable Coil System FDA UDI
Identifiers
- Catalog Number
- CDF10061630 FDA UDI
- Primary DI / UDI-DI
- 00878528007357 FDA UDI
- 510(k) Number
- K080437 FDA UDI
- FDA Product Code
- HCG FDA UDI
- GMDN Term
- Neurovascular embolization coil FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5950 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Deltapaq Cerecyte by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (1)
- FDA UDI f7439566-489d-49d6-a5b4-8ba3e97d5d49 38 fields · synced Jun 1, 2026