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Vaccess

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Vaccess FDA UDI
Generic Name
Vascular port/catheter FDA UDI
Device Name
Vaccess CT Low-Profile Power-Injectable Implantable Port 6F (without Suture Plugs) (6F) FDA UDI
Model / Reference
7360001 FDA UDI
Description
Vaccess CT Low-Profile Power-Injectable Implantable Port 6F (without Suture Plugs) (6F) FDA UDI

Identifiers

Catalog Number
7360001 FDA UDI
Primary DI / UDI-DI
00801741027444 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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 60 Centimeter FDA UDI
Catheter Gauge — 6 French FDA UDI

Category: Vascular port/catheter

Vaccess by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular port/catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Access Systems, Inc.

Sources (1)

  • FDA UDI 968fcee8-c63c-4722-8c14-93f90be5518b 36 fields · synced Jun 9, 2026