NA
- Primary DI
- 20763000871837
- Brand
- NA
- Company
- MEDTRONIC, INC.
- Model
- AFR-00007
- Device description
- PATCH AFR-00007 LOCATION REF 4PK 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
- true
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 |
|---|
| 20763000871837 | Package | GS1 | 4 | In Commercial Distribution |
| 00763000871833 | Primary | GS1 | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Cardiac mapping system reference patch | A component of a cardiac mapping system that is an adhesive device placed on the surface of a patient's body, typically the chest and/or back, to provide a fixed reference point for the tip of an internal, non-fluoroscopic catheter during an electrophysiological and electromechanical real-time mapping of the heart. It may be sensor-containing or have a sensor attached to it, and is used to compensate for patient movement during the procedure. It is typically used with a cardiac mapping system computer to assist in the location and navigation of the catheter tip, and to provide electrocardiogram information. This is a single-use device. |
Storage And Handling
| Type | Low | High | Condition |
|---|
| Special Storage Condition, Specify | 0 | 0 | Keep dry |
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
- true
- 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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