FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00763000245030 · Model: 37642 · MEDTRONIC, INC.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00763000245030
Version / Model
37642
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-23
Public Version
2
Public Version Date
2020-07-07
Public Version Status
Update
Public Device Record Key
1ac64672-74cc-412f-92df-c1b7220bd375

Device Description

PROG 37642 PATIENT ACTIVA US PAPER EN

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
MRU implanted subcortical electrical Stimulator (motor disorders)
MHY STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
NHL Stimulator, electrical, implanted, for parkinsonian symptoms
OLM Deep brain stimulator for obsessive compulsive disorder (OCD)
PJS Stimulator, electrical, implanted, for essential tremor

GMDN Terms

Code Name
61393 Multiple active implantable device programmer

Identifiers

Type ID
Primary 00763000245030

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P960009 229

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-30 – 135 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
-34 – 57 Degrees Celsius