Identity
- Trade Name
- Vortex FDA UDI
- Generic Name
- Vascular port/catheter FDA UDI
- Device Name
- Vortex MP Low Profile Titanium Port System with Attachable 5F x 76cm Silicone Catheter FDA UDI
- Model / Reference
- MP-P5SDT FDA UDI
- Description
- Vortex MP Low Profile Titanium Port System with Attachable 5F x 76cm Silicone Catheter FDA UDI
Identifiers
- Primary DI / UDI-DI
- H787MPP5SDT0 FDA UDI
- 510(k) Number
- K033473 FDA UDI
- FDA Product Code
- LJT FDA UDI
- GMDN Term
- Vascular port/catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5965 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Dimensions & Sizes
- Size
- Length — 76 Centimeter FDA UDINeedle Gauge — 18 Gauge FDA UDILumen/Inner Diameter — 0.9 Millimeter FDA UDICatheter Gauge — 5 French FDA UDIOuter Diameter — 1.7 Millimeter FDA UDI
Category: Vascular port/catheter
Vortex by Navilyst Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Vascular port/catheter.
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- Vital-Port — COOK INCORPORATED · Class II
- PowerPort — Bard Access Systems, Inc. · Class II
- Deltec — ICU MEDICAL, INC. · Class II
- PowerPort ClearVUE — Bard Access Systems, Inc. · Class II
Cleared under the same submission
K033473 also covers:
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 II | Pending data |
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Manufacturer
- Manufacturer
- Navilyst Medical, Inc.
Sources (1)
- FDA UDI 8350d721-78d9-4ab0-84c2-7b00bf549eda 36 fields · synced May 30, 2026