Identity
- Trade Name
- Current® FDA UDI
- Generic Name
- Dual-chamber implantable defibrillator FDA UDI
- Device Name
- Tiered-therapy cardioverter/defibrillatorVVED DDDR FDA UDI
- Model / Reference
- 2107-36 FDA UDI
- Description
- Tiered-therapy cardioverter/defibrillatorVVED DDDR FDA UDI
Identifiers
- Catalog Number
- 2107-36 FDA UDI
- Primary DI / UDI-DI
- 05414734502207 FDA UDI
- FDA Product Code
- NVZ FDA UDI
- GMDN Term
- Dual-chamber implantable defibrillator FDA UDI
Classification
- Device Class
- Class III 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 39 Milliliter FDA UDI
Category: Dual-chamber implantable defibrillator
Current® by St. Jude Medical, Inc. — Class III — 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 III | Pending data |
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Manufacturer
- Manufacturer
- St. Jude Medical, Inc.
Sources (1)
- FDA UDI dc8900aa-c56b-4f36-b958-5921f7388362 37 fields · synced Jun 1, 2026