Port Access

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name: Port Access FDA UDI
Generic Name: Vascular port administration set FDA UDI
Device Name: AllPoints Port Access System PowerLoc Max 20G x 0.75 inch FDA UDI
Model / Reference: AN142075 FDA UDI
Description: AllPoints Port Access System PowerLoc Max 20G x 0.75 inch FDA UDI

Identifiers

Catalog Number: AN142075 FDA UDI
Primary DI / UDI-DI: 00801741119224 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

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

Category: Vascular port administration set

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

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Infusion Safety Products, Inc. — Infusion Safety Products, Inc. · Class II
VYGON — Vygon Corp. · Class II
All-Med, Inc. — ALL-MED INC · Class II
PORT ACCESS INFUSION SET — SB-KAWASUMI LABORATORIES, 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: Bard Access Systems, Inc.

Sources (1)

FDA UDI dc94dbf9-0610-467c-9fbd-ae9f3c8d4b64 37 fields · synced Jun 9, 2026