Identity
- Trade Name
- Sprint Quattro Secure® DXAC/DSP FDA UDI
- Generic Name
- Endocardial defibrillation lead FDA UDI
- Device Name
- LEAD 694758 SPRINT US 58CM FPA QUAD FDA UDI
- Model / Reference
- 694758 FDA UDI
- Description
- LEAD 694758 SPRINT US 58CM FPA QUAD FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00613994740915 FDA UDI
- FDA Product Code
- DTB FDA UDINVY FDA UDILWS FDA UDI
- GMDN Term
- Endocardial defibrillation lead FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 870.3680 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
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 58.0 Centimeter FDA UDI
Sprint Quattro Secure® DXAC/DSP by Medtronic, Inc. — Class III — 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 III | Pending data |
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Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI 137fa8b2-646c-4df7-9ac7-409f36bb91ee 37 fields · synced May 31, 2026