Identity
- Trade Name
- Intercept™ FDA UDI
- Generic Name
- Multiple active implantable device programmer FDA UDI
- Device Name
- PROG 37441 INTERCEPT DBS REFURB US FDA UDI
- Model / Reference
- 37441-RFB FDA UDI
- Description
- PROG 37441 INTERCEPT DBS REFURB US FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000875602 FDA UDI
- PMA Number
- P960009 FDA UDI
- FDA Product Code
- MBX FDA UDI
- GMDN Term
- Multiple active implantable device programmer FDA UDI
Classification
- Device Class
- Class III 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: Multiple active implantable device programmer
Intercept™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Multiple active implantable device programmer.
- Wearable Antenna Assembly/StimQ Wearable Antenna Gear — STIMWAVE TECHNOLOGIES INCORPORATED · Class II
- HeartMate Touch™ — Thoratec Corp · Class III
- SJM™ — ST. JUDE MEDICAL, INC. · Class III
- Genesis™ — ST. JUDE MEDICAL, INC. · Class III
- SeaSilk Antenna Large 28" Length — STIMWAVE TECHNOLOGIES INCORPORATED · Class II
- SJM MRI Activator™ — ST. JUDE MEDICAL, INC. · Class III
- Large Antenna 30" Length — STIMWAVE TECHNOLOGIES INCORPORATED · Class II
- Merlin™ — ST. JUDE MEDICAL, INC. · Class III
Cleared under the same submission
P960009 also covers:
- Activa® PC — MEDTRONIC, INC.
- Activa® RC — MEDTRONIC, INC.
- Activa® RC — MEDTRONIC, INC.
- Assess ® — MEDTRONIC, INC.
- DBS™ — MEDTRONIC, INC.
- DBS™ — MEDTRONIC, INC.
- Intercept ™ — MEDTRONIC, INC.
- N'VISION 8840 — MEDTRONIC, INC.
- Percept™ PC BrainSense™ — MEDTRONIC, INC.
- SenSight™ — MEDTRONIC, INC.
- SenSight™ — MEDTRONIC, INC.
- SenSight™ — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI 0666d127-bb98-49cb-a628-43cf15e61781 36 fields · synced Jun 8, 2026