FDA UDI In Commercial Distribution 🇺🇸 United States

Assess Review ™

DI: 00613994808349 · Model: 7438 · MEDTRONIC, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Assess Review ™
Primary DI
00613994808349
Version / Model
7438
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
4
Public Version Date
2023-07-31
Public Version Status
Update
Public Device Record Key
5997f3d9-149d-442c-811d-abaef1b41dc7

Device Description

PROG 7438 SOLETRA EZ PATIENT US

Device Characteristics

Single Use
No
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
Labeling does not contain MRI Safety Information
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
No
Sterilization Prior Use
No

Product Codes

Code Name
OLM Deep brain stimulator for obsessive compulsive disorder (OCD)
MRU implanted subcortical electrical Stimulator (motor disorders)
MHY STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
MFR Stimulator, brain, implanted, for behavior modification
NHL STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS
PJS Stimulator, electrical, implanted, for essential tremor

GMDN Terms

Code Name
61393 Multiple active implantable device programmer

Identifiers

Type ID
Primary 00613994808349

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P960009 080