Alaris

FDA UDI

Class II (US FDA UDI)

by CareFusion 303, INC

Identity

Trade Name: Alaris FDA UDI
Generic Name: Barcode reader FDA UDI
Device Name: Alaris Auto-ID Module (R V8) FDA UDI
Model / Reference: 8600 FDA UDI
Description: Alaris Auto-ID Module (R V8) FDA UDI

Identifiers

Primary DI / UDI-DI: 10885403517730 FDA UDI
FDA Product Code: FRN FDA UDI
GMDN Term: Barcode reader FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5725 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Barcode reader

Alaris by CareFusion 303, INC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: CareFusion 303, INC

Sources (1)

FDA UDI a3f5100c-3bdb-428e-ae1d-4c431b0a1384 35 fields · synced May 30, 2026