Identity
- Trade Name
- REVOLUTION FDA UDI
- Generic Name
- Centrifugal circulatory assist pump, electric FDA UDI
- Model / Reference
- REVOLUTION FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08033178104777 FDA UDI
- 510(k) Number
- K011835 FDA UDI
- FDA Product Code
- KFM FDA UDI
- GMDN Term
- Centrifugal circulatory assist pump, electric FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4360 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
Category: Centrifugal circulatory assist pump, electric
Revolution by Sorin Group Italia Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Centrifugal circulatory assist pump, electric.
- CAPIOX® SP PUMP — Terumo Corp. · Class II
- CAPIOX® SP PUMP — Terumo Corp. · Class II
- REVOLUTION — SORIN GROUP ITALIA SRL · Class II
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 |
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Manufacturer
- Manufacturer
- Sorin Group Italia Srl
Sources (1)
- FDA UDI f2d0ebaa-6571-4472-9187-1ccc4b04d122 32 fields · synced Jun 8, 2026