AllPoints Port Access System MiniLoc

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name: AllPoints Port Access System MiniLoc FDA UDI
Generic Name: Peripheral angioplasty balloon catheter, basic FDA UDI
Device Name: AllPoints Port Access System MiniLoc 20G x 0.75 inch + BioPatch FDA UDI
Model / Reference: AN632034B FDA UDI
Description: AllPoints Port Access System MiniLoc 20G x 0.75 inch + BioPatch FDA UDI

Identifiers

Catalog Number: AN632034B FDA UDI
Primary DI / UDI-DI: 00801741215346 FDA UDI
FDA Product Code: FPA FDA UDI
GMDN Term: Peripheral angioplasty balloon catheter, basic 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: Length — 0.75 Inch FDA UDI
Needle Gauge — 20 Gauge FDA UDI

Category: Peripheral angioplasty balloon catheter, basic

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

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Also classified as Peripheral angioplasty balloon catheter, basic.

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Armada — Abbott Vascular · 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 587c8299-a411-44d0-b9b1-7130643e3965 37 fields · synced Jun 9, 2026