FDA UDI In Commercial Distribution 🇺🇸 United States

Prometra Programmer

DI: 00810335020167 · Model: 12828 · Flowonix Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prometra Programmer
Primary DI
00810335020167
Version / Model
12828
Company Name
Flowonix Medical, Inc.
Labeler DUNS
013518517
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-04-29
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d385c0fd-c2c9-4703-9930-fba279e7c809

Device Description

The Prometra Programmer is a non-sterile handheld menu driven device, external to the implanted pump that enables remote programming of the implantable Programmable Pump using a touchscreen interface. The Programmer can program the pump to deliver a precise flow of medication at a constant or variable rate, or it can be set to periodically deliver a drug dosage at distinct intervals of time (i.e., Periodic Flow Mode). There is also an option to interrupt the pump's current medication regimen and deliver an immediate infusion of medication (Demand Bolus).

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
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LKK Pump, Infusion, Implanted, Programmable

GMDN Terms

Code Name
44074 Infusion pump programmer

Identifiers

Type ID
Primary 00810335020167

Premarket Submissions

Submission Number Supplement Number
P080012 021

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not get wet