Identity
- Trade Name
- CareLink SmartSync™ FDA UDI
- Generic Name
- Implantable pacemaker analyser, intraoperative FDA UDI
- Device Name
- PROGRAMMER 24970A US MKT BASE ONLY FDA UDI
- Model / Reference
- 24970A FDA UDI
- Description
- PROGRAMMER 24970A US MKT BASE ONLY FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000201289 FDA UDI
- PMA Number
- P890003 FDA UDI
- FDA Product Code
- DTA FDA UDIDTC FDA UDI
- GMDN Term
- Implantable pacemaker analyser, intraoperative FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.3720 FDA UDI870.3630 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Implantable pacemaker analyser, intraoperative
CareLink SmartSync™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Implantable pacemaker analyser, intraoperative.
- Renamic PSA Module — BIOTRONIK SE & Co. KG · Class III
- CareLink SmartSync™ — MEDTRONIC, INC. · Class II
- CareLink SmartSync™ — MEDTRONIC, INC. · Class II
- CareLink SmartSync™ — MEDTRONIC, INC. · Class II
Cleared under the same submission
P890003 also covers:
- CAPSURE® VDD-2 — MEDTRONIC, INC.
- CARELINK® MONITOR — MEDTRONIC, INC.
- CardioSight™ Reader — MEDTRONIC, INC.
- CareLink SmartSync™ PSA Application — MEDTRONIC, INC.
- Instrument Command Library — MEDTRONIC, INC.
- Medtronic CareLink® Programmer — MEDTRONIC, INC.
- MyCareLink™ — MEDTRONIC, INC.
- MyCareLink™ — MEDTRONIC, INC.
- MyCareLink™ — MEDTRONIC, INC.
- MyCareLink™ — MEDTRONIC, INC.
- MyCareLink™ — MEDTRONIC, INC.
- MyCareLink™ — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI d80965f5-0c7b-4ad3-b98a-ce8bf6f42a51 36 fields · synced May 29, 2026