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AllPoints

FDA UDI

Class I (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
AllPoints FDA UDI
Generic Name
Vascular catheterization support/maintenance kit, non-medicated FDA UDI
Device Name
AllPoints Dressing Change System with Fixed Post Statlock and BioPatch FDA UDI
Model / Reference
APDCSFB1 FDA UDI
Description
AllPoints Dressing Change System with Fixed Post Statlock and BioPatch FDA UDI

Identifiers

Catalog Number
APDCSFB1 FDA UDI
Primary DI / UDI-DI
00801741137570 FDA UDI
FDA Product Code
KMK FDA UDI
GMDN Term
Vascular catheterization support/maintenance kit, non-medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5210 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular catheterization support/maintenance kit, non-medicated

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

Similar devices

Also classified as Vascular catheterization support/maintenance kit, non-medicated.

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 8bea44b5-e800-4356-8d9e-809af4159ae1 36 fields · synced Jun 9, 2026