FDA UDI In Commercial Distribution 🇺🇸 United States

Intellis™ Pro

DI: 00763000984656 · Model: 977118 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Intellis™ Pro
Primary DI
00763000984656
Version / Model
977118
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-19
Public Version
2
Public Version Date
2025-12-16
Public Version Status
Update
Public Device Record Key
c7e90529-d25e-4ed1-a79e-3234b78de66d

Device Description

INS 977118 INTELLIS PRO US EMANUAL

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
QRB Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy
LGW Stimulator, spinal-cord, totally implanted for pain relief

GMDN Terms

Code Name
64970 Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable

Identifiers

Type ID
Primary 00763000984656

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P840001 591