Identity
- Trade Name
- Prometra Catheter Revision Kit FDA UDI
- Generic Name
- Spinal infusion/drainage catheter FDA UDI
- Device Name
- The Catheter Revision Kit is a sterile kit designed to facilitate the replacement of a section of the intrathecal catheter. A replacement catheter segment is provided with a catheter connector (and sleeve) to allow this segment to be attached to the existing catheter. FDA UDI
- Model / Reference
- 11830 FDA UDI
- Description
- The Catheter Revision Kit is a sterile kit designed to facilitate the replacement of a section of the intrathecal catheter. A replacement catheter segment is provided with a catheter connector (and sleeve) to allow this segment to be attached to the existing catheter. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810335020105 FDA UDI
- PMA Number
- P080012 FDA UDI
- FDA Product Code
- LKK FDA UDI
- GMDN Term
- Spinal infusion/drainage catheter FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Spinal infusion/drainage catheter
Prometra Catheter Revision Kit by Flowonix Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Spinal infusion/drainage catheter.
- SPINAUT-E — IMEDICOM CO., LTD. · Class II
- SPINAUT-E — IMEDICOM CO., LTD. · Class II
- SPINAUT-E — IMEDICOM CO., LTD. · Class II
- SPINAUT-E — IMEDICOM CO., LTD. · Class II
- Video Guided Catheter — Myelotec, Inc. · Class II
- SPINAUT-E — IMEDICOM CO., LTD. · Class II
- SPINAUT-V — IMEDICOM CO., LTD. · Class II
- Video Guided Catheter — Myelotec, Inc. · Class II
Cleared under the same submission
P080012 also covers:
- Prometra Catheter Access 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 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Flowonix Medical, Inc.
Sources (1)
- FDA UDI 6c58e37c-137b-488f-a564-7fd2db38a357 35 fields · synced Jun 6, 2026