← Back to catalogue

NorPort Vascular Access Port

FDA UDI

Class II (US FDA UDI)

by Norfolk Medical

Identity

Trade Name
NorPort Vascular Access Port FDA UDI
Generic Name
Infusion/injection port, implantable FDA UDI
Device Name
Low-Profile Titanium NorPort Vascular Access Port with 5F preattached Silicone Catheter and Standard Introducer Kit FDA UDI
Model / Reference
NorPort FDA UDI
Description
Low-Profile Titanium NorPort Vascular Access Port with 5F preattached Silicone Catheter and Standard Introducer Kit FDA UDI

Identifiers

Catalog Number
NP21211K FDA UDI
Primary DI / UDI-DI
M991NP21211K1 FDA UDI
FDA Product Code
LJT FDA UDI
GMDN Term
Infusion/injection port, implantable 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

No

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Total Volume — 0.321 Milliliter FDA UDI

Category: Infusion/injection port, implantable

NorPort Vascular Access Port by Norfolk Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infusion/injection port, implantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Norfolk Medical

Sources (1)

  • FDA UDI fd064cc6-07c5-4f4e-8666-4c4ff7fe164f 36 fields · synced Jun 6, 2026