Identity
- Trade Name
- SenSight™ FDA UDI
- Generic Name
- Deep brain electrical stimulation system FDA UDI
- Device Name
- LEAD B3300533 SENSIGHT 0.5MM EMAN LJ53 FDA UDI
- Model / Reference
- B3300533 FDA UDI
- Description
- LEAD B3300533 SENSIGHT 0.5MM EMAN LJ53 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000426378 FDA UDI
- FDA Product Code
- MBX FDA UDIMRU FDA UDINHL FDA UDIMHY FDA UDIPJS FDA UDI
- GMDN Term
- Deep brain electrical stimulation system 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
Yes
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
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Length — 33.0 Centimeter FDA UDI
Category: Deep brain electrical stimulation system
SenSight™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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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 |
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Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI 91e08b44-537f-4218-81e8-7fef866fc4c3 36 fields · synced May 30, 2026