Identity
- Trade Name
- Consulta® CRT-P FDA UDI
- Generic Name
- Cardiac resynchronization therapy implantable pacemaker FDA UDI
- Device Name
- CRT C4TR01 CONSULTA CRT-P US MR FDA UDI
- Model / Reference
- C4TR01 FDA UDI
- Description
- CRT C4TR01 CONSULTA CRT-P US MR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00613994713667 FDA UDI
- PMA Number
- P010015 FDA UDI
- FDA Product Code
- NVZ FDA UDINKE FDA UDI
- GMDN Term
- Cardiac resynchronization therapy implantable pacemaker 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cardiac resynchronization therapy implantable pacemaker
Consulta® CRT-P by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiac resynchronization therapy implantable pacemaker.
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Cleared under the same submission
P010015 also covers:
- ATTAIN® BIPOLAR OTW — MEDTRONIC, INC.
- CareLink SmartSync™ Percepta Serena Solara Application — MEDTRONIC, INC.
- Percepta™ CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Percepta™ CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Percepta™ Quad CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Percepta™ Quad CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Serena™ CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Serena™ CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Serena™ Quad CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Serena™ Quad CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Solara™ CRT-P MRI SureScan™ — MEDTRONIC, INC.
- Solara™ CRT-P MRI SureScan™ — MEDTRONIC, INC.
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 ee35bcab-7776-4675-94f9-d63ab466f7c2 36 fields · synced May 31, 2026