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T-Port

FDA UDI

Class II (US FDA UDI)

by Pfm Medical Incorporated

Identity

Trade Name
T-Port FDA UDI
Generic Name
Vascular port/catheter FDA UDI
Device Name
T-Port PUR Kit HF with 8F x 750 mm Attachable Polyurethane Catheter FDA UDI
Model / Reference
616.365.2080-A FDA UDI
Description
T-Port PUR Kit HF with 8F x 750 mm Attachable Polyurethane Catheter FDA UDI

Identifiers

Primary DI / UDI-DI
07640110987247 FDA UDI
510(k) Number
K073210 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

Yes

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

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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1e43e126-f8fe-43b8-9163-70a75e65271e 35 fields · synced May 30, 2026