Identity
- Trade Name
- T-Port FDA UDI
- Generic Name
- Vascular port/catheter FDA UDI
- Device Name
- 8F T-Port LP HP PUR Kit FDA UDI
- Model / Reference
- 611.366.2088-HAV FDA UDI
- Description
- 8F T-Port LP HP PUR Kit FDA UDI
Identifiers
- Catalog Number
- 611.366.2088-HAV FDA UDI
- Primary DI / UDI-DI
- 00813623010789 FDA UDI
- FDA Product Code
- PXK 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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
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: Vascular port/catheter
T-Port by Pfm Medical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vascular port/catheter.
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- PowerPort M.R.I. — Bard Access Systems, Inc. · Class II
- Vital-Port — COOK INCORPORATED · Class II
- Vortex — NAVILYST MEDICAL, INC. · Class II
- PowerPort — Bard Access Systems, Inc. · Class II
- Deltec — ICU MEDICAL, INC. · Class II
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
- Pfm Medical Incorporated
Sources (1)
- FDA UDI 56c10e2e-f1c4-44c1-a7c2-99957b70d47b 35 fields · synced Jun 1, 2026