Identity
- Trade Name
- Surge Cardiovascular FDA UDI
- Generic Name
- Implantable ventricular circulatory assist system FDA UDI
- Device Name
- PEAK Left Ventricular Vent Cannula, 16 Fr FDA UDI
- Model / Reference
- LVV-016S FDA UDI
- Description
- PEAK Left Ventricular Vent Cannula, 16 Fr FDA UDI
Identifiers
- Catalog Number
- LVV-016S FDA UDI
- Primary DI / UDI-DI
- 00817278012211 FDA UDI
- FDA Product Code
- DWF FDA UDI
- GMDN Term
- Implantable ventricular circulatory assist system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4210 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Category: Implantable ventricular circulatory assist system
Surge Cardiovascular by Med Michigan Holdings Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Med Michigan Holdings Llc
Sources (1)
- FDA UDI 0096dc17-7d8c-4071-9cea-e4321d411b7b 34 fields · synced May 30, 2026