FDA UDI In Commercial Distribution 🇺🇸 United States

SenSight™

DI: 00763000426408 · Model: B3300542M · MEDTRONIC, INC.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SenSight™
Primary DI
00763000426408
Version / Model
B3300542M
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-05
Public Version
2
Public Version Date
2025-12-16
Public Version Status
Update
Public Device Record Key
b7196b88-e8e1-43a3-99d9-e5e5a40fb3c6

Device Description

LEAD B3300542M SENSIGHT 0.5MM EMAN LJ53

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBX Stimulator, thalamic, epilepsy, implanted
NHL Stimulator, electrical, implanted, for parkinsonian symptoms
MRU implanted subcortical electrical Stimulator (motor disorders)
PJS Stimulator, electrical, implanted, for essential tremor
MHY Stimulator, electrical, implanted, for parkinsonian tremor

GMDN Terms

Code Name
37307 Deep brain electrical stimulation system

Identifiers

Type ID
Primary 00763000426408

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
H020007 285
P960009 391

Device Sizes

Type Value Unit Text
Length 42.0 Centimeter