Identity
- Trade Name
- RF CONDUCTR™ MC FDA UDI
- Generic Name
- Cardiac radio-frequency ablation system catheter FDA UDI
- Device Name
- CATH 0786042 RF CONDUCTR W/O CE FDA UDI
- Model / Reference
- 0786042 FDA UDI
- Description
- CATH 0786042 RF CONDUCTR W/O CE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00643169148123 FDA UDI
- PMA Number
- P930029 FDA UDI
- FDA Product Code
- LPB FDA UDI
- GMDN Term
- Cardiac radio-frequency ablation system catheter 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
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cardiac radio-frequency ablation system catheter
Rf Conductr™ Mc by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
P930029 also covers:
- ATAKR® II — MEDTRONIC, INC.
- RF CONDUCTR™ MC — MEDTRONIC, INC.
- RF CONDUCTR™ MC — MEDTRONIC, INC.
- RF Conductr™ MC — MEDTRONIC, INC.
- RF Conductr™ MC — MEDTRONIC, INC.
- RF ENHANCR® II — MEDTRONIC, INC.
- RF ENHANCR® II — MEDTRONIC, INC.
- RF ENHANCR® II — MEDTRONIC, INC.
- RF Enhancr™ II — MEDTRONIC, INC.
- RF Enhancr™ II — MEDTRONIC, INC.
- RF Enhancr™ II — MEDTRONIC, INC.
- RF Enhancr™ II — 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 9c113e66-c457-4dac-9028-61231a9439f3 37 fields · synced May 29, 2026