NA
- Primary DI
- 00763000871987
- Brand
- NA
- Company
- MEDTRONIC, INC.
- Model
- AFR-00013
- Device description
- CART AFR-00013 SYSTEM US
- Published
- 2024-10-21
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| DQK | Computer, diagnostic, programmable |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| DQK | Computer, Diagnostic, Programmable | Cardiovascular | 2 |
Premarket Details
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|
| K233943 | 000 | Affera Mapping System (AFR-00003); Location Reference Patch Kit (AFR-00007); System Cart (AFR-00013) | Medtronic, Inc. | 2024-03-08 | DQK |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00763000871987 | Primary | GS1 | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Cardiac mapping system | An assembly of devices designed to measure, process, and store electronic data for the interpretation of cardiac physiological parameters received from the output of connected measuring devices (e.g., body surface or intracardiac electrocardiograph (ECG) sensors, transducers, and catheters). The measurements can be compared to pre-established diagnostic criteria for parameters such as cardiac blood flow, electrical conduction, or heart chamber geometry. It typically consists of dedicated workstation, hardware and software that display real-time, three-dimensional (3-D) cardiac maps (e.g., electrical propagation, electrical potential, and cardiac chamber geometry maps), and a catheter. |
Contacts
| Phone | Email |
|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags
- DUNS number
- 006261481
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 00195278343512 | CARESCAPE CENTRAL STATION | Ge Medical Systems Information Technologies, Inc. | DQK | 2026-02-11 |
| 00851424007089 | VIVO | Catheter Precision, Inc. | DQK | 2026-02-03 |
| 00085142400710 | VIVO Positioning Patches | Catheter Precision, Inc. | DQK | 2026-02-03 |
| 00851424007119 | VIVO System | Catheter Precision, Inc. | DQK | 2026-02-03 |
| 05415067055613 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2026-01-08 |
| 05415067054883 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2025-12-19 |
| 00732094360295 | Welch Allyn, Inc. | WELCH ALLYN, INC. | DQK | 2025-12-18 |
| 05415067053435 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2025-12-17 |
| 05415067053503 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2025-12-17 |
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| 05415067055231 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2025-12-17 |
| 05415067055248 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2025-12-17 |
| 00850012226291 | iMap 3D Mapping and Navigation System | Cardionxt Inc | DQK | 2025-12-10 |
| 05415067051219 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2025-12-08 |
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| 03770019196069 | Volta AF-Xplorer II | SUBSTRATE HD | DQK | 2025-11-18 |
| 00763000998394 | N/A | MEDTRONIC, INC. | DQK | 2025-11-14 |
| 05415067051158 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2025-09-15 |
| 05415067051172 | EnSite™ | ST. JUDE MEDICAL, INC. | DQK | 2025-09-15 |