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Port Access Kit

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Port Access Kit FDA UDI
Generic Name
Vascular port administration set FDA UDI
Device Name
Port Access Kit MiniLoc 20G x 0.75 inch with y-site FDA UDI
Model / Reference
2682034 FDA UDI
Description
Port Access Kit MiniLoc 20G x 0.75 inch with y-site FDA UDI

Identifiers

Catalog Number
2682034 FDA UDI
Primary DI / UDI-DI
00801741044656 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Vascular port administration set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

Yes

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

Dimensions & Sizes

Size
Length — 0.75 Inch FDA UDI
Needle Gauge — 20 Gauge FDA UDI

Category: Vascular port administration set

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

Similar devices

Also classified as Vascular port administration set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1a712635-849b-47ef-9564-b53b906185a0 37 fields · synced Jun 9, 2026