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Alaris

FDA UDI

Class II (US FDA UDI)

by CareFusion 303, INC

Identity

Trade Name
Alaris FDA UDI
Generic Name
Infusion pump medication-dosage application software FDA UDI
Device Name
Calculation Services 1.X FDA UDI
Model / Reference
1.X FDA UDI
Description
Calculation Services 1.X FDA UDI

Identifiers

Primary DI / UDI-DI
10885403510489 FDA UDI
FDA Product Code
PHC FDA UDI
GMDN Term
Infusion pump medication-dosage application software 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Infusion pump medication-dosage application software

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

Similar devices

Also classified as Infusion pump medication-dosage application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CareFusion 303, INC

Sources (1)

  • FDA UDI f8e757e2-45cd-40cf-ae46-92fc16473744 34 fields · synced May 29, 2026