Identity
- Trade Name
- Prometra Programmer FDA UDI
- Generic Name
- Infusion pump programmer FDA UDI
- Device Name
- 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). FDA UDI
- Model / Reference
- 12828 FDA UDI
- 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). FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810335020167 FDA UDI
- PMA Number
- P080012 FDA UDI
- FDA Product Code
- LKK FDA UDI
- GMDN Term
- Infusion pump programmer FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Infusion pump programmer
Prometra Programmer by Flowonix Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Infusion pump programmer.
- Prometra Patient Therapy Controller — Flowonix Medical, Inc. · Class III
- Prometra Physician Configuration Device — Flowonix Medical, Inc. · Class III
- Prometra Clinical Programmer — Flowonix Medical, Inc. · Class III
- Prometra Clinician Programmer Print Tool — Flowonix Medical, Inc. · Class III
- Prometra Programmer — Flowonix Medical, Inc. · Class III
Cleared under the same submission
P080012 also covers:
- Prometra Catheter Access Kit — Flowonix Medical, Inc.
- Prometra Catheter Revision Kit — Flowonix Medical, Inc.
- Prometra Clinical Programmer — Flowonix Medical, Inc.
- Prometra Clinician Programmer Print Tool — Flowonix Medical, Inc.
- Prometra II Pump — Flowonix Medical, Inc.
- Prometra Intrathecal Catheter — Flowonix Medical, Inc.
- Prometra Patient Therapy Controller — Flowonix Medical, Inc.
- Prometra Physician Configuration Device — Flowonix Medical, Inc.
- Prometra Programmable Pump — Flowonix Medical, Inc.
- Prometra Programmable Pump — Flowonix Medical, Inc.
- Prometra Programmer — Flowonix Medical, Inc.
- Prometra Refill Kit — Flowonix Medical, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Flowonix Medical, Inc.
Sources (1)
- FDA UDI d385c0fd-c2c9-4703-9930-fba279e7c809 35 fields · synced May 30, 2026