FDA UDI In Commercial Distribution 🇺🇸 United States

Prometra Programmable Pump

DI: 00810335020082 · Model: 11827 · Flowonix Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prometra Programmable Pump
Primary DI
00810335020082
Version / Model
11827
Company Name
Flowonix Medical, Inc.
Labeler DUNS
013518517
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
4
Public Version Date
2018-10-22
Public Version Status
Update
Public Device Record Key
e09049d7-8a0f-4939-8708-743af0a54551

Device Description

The Prometra Programmable Pump is a sterile, battery-operated, teardrop-shaped implantable, programmable infusion pump, with a rigid titanium housing and flow controller system, which dispenses infusate into the intrathecal space through an implanted intrathecal catheter.

Device Characteristics

Single Use
Yes
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 Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LKK Pump, Infusion, Implanted, Programmable

GMDN Terms

Code Name
46024 Implantable intrathecal infusion pump, programmable

Identifiers

Type ID
Primary 00810335020082

Premarket Submissions

Submission Number Supplement Number
P080012 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 52 Degrees Celsius