FDA UDI In Commercial Distribution 🇺🇸 United States

Tester

DI: 20643169975105 · Model: MMT-7736L · MEDTRONIC MINIMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
Tester
Primary DI
20643169975105
Version / Model
MMT-7736L
Company Name
MEDTRONIC MINIMED, INC.
Labeler DUNS
849626338
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2019-03-07
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
edac7ceb-043c-40fc-bc16-3f735a96063e

Device Description

PLUG MMT-7736L TEST LOCKOUT 2PK EN

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
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
OZP Automated insulin dosing device system, single hormonal control

GMDN Terms

Code Name
44611 Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Identifiers

Type ID
Primary 20643169975105
Unit of Use 00643169975101

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P160017 003

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-20 – 5 Degrees Celsius