FDA UDI In Commercial Distribution 🇺🇸 United States

Eversense DMS Pro

DI: 00817491023513 · Model: FG-5905-01-300 · SENSEONICS, INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Eversense DMS Pro
Primary DI
00817491023513
Version / Model
FG-5905-01-300
Catalog Number
FG-5905-01-300
Company Name
SENSEONICS, INCORPORATED
Labeler DUNS
966865636
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-10
Public Version
1
Public Version Date
2022-03-18
Public Version Status
New
Public Device Record Key
4440403f-23ed-4bab-a2c3-d35c344735c5

Device Description

The Eversense DMS Pro is a software intended for clinic use. Eversense DMS Pro can be used to review and evaluate historical glucose data from compatible devices and systems.

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
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
PHV Continuous Glucose Monitor Retrospective Data Analysis Software

GMDN Terms

Code Name
61915 Implantable glucose monitoring system

Identifiers

Type ID
Primary 00817491023513

Customer Contacts

Phone
844-736-7348