Identity
- Trade Name
- Viva™ Quad XT CRT-D FDA UDI
- Generic Name
- Cardiac resynchronization therapy implantable defibrillator FDA UDI
- Device Name
- CRTD DTBA1QQ VIVAQUADXT US IS4/DF4 FDA UDI
- Model / Reference
- DTBA1QQ FDA UDI
- Description
- CRTD DTBA1QQ VIVAQUADXT US IS4/DF4 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000059651 FDA UDI
- FDA Product Code
- NIK FDA UDIKRG FDA UDI
- GMDN Term
- Cardiac resynchronization therapy implantable defibrillator FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 870.3700 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cardiac resynchronization therapy implantable defibrillator
Viva™ Quad XT CRT-D by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiac resynchronization therapy implantable defibrillator.
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- Unify Quadra™ — ST. JUDE MEDICAL, INC. · Class III
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 ceed6d8a-50f1-4d84-bc24-db3240232920 35 fields · synced May 30, 2026