FDA UDI In Commercial Distribution 🇺🇸 United States

MiniMed™ Mobile

DI: 00763000416676 · Model: MMT-6102 · MEDTRONIC MINIMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MiniMed™ Mobile
Primary DI
00763000416676
Version / Model
MMT-6102
Company Name
MEDTRONIC MINIMED, INC.
Labeler DUNS
849626338
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-06
Public Version
5
Public Version Date
2023-07-13
Public Version Status
Update
Public Device Record Key
00bee004-c651-47bd-85b2-b58deefe9a8c

Device Description

SFTWR MMT-6102 AHCL APP 1.3.3 IOS

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
PKU Insulin pump secondary display

GMDN Terms

Code Name
58884 Self-care monitoring/reporting software

Identifiers

Type ID
Primary 00763000416676

Customer Contacts