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Alaris™ PCA Module, Model 8120

FDA UDI

Class II (US FDA UDI)

by CareFusion 303, INC

Identity

Trade Name
Alaris™ PCA Module, Model 8120 FDA UDI
Generic Name
Bedside syringe pump FDA UDI
Device Name
Alaris™ PCA Module, Model 8120 v12.3.0 FDA UDI
Model / Reference
8120 FDA UDI
Description
Alaris™ PCA Module, Model 8120 v12.3.0 FDA UDI

Identifiers

Catalog Number
8120BDXEN123 FDA UDI
Primary DI / UDI-DI
10885403516030 FDA UDI
FDA Product Code
MEA FDA UDI
GMDN Term
Bedside syringe pump 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Bedside syringe pump

Alaris™ PCA Module, Model 8120 by CareFusion 303, INC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedside syringe pump.

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 84a2d508-c8cc-4907-a0b2-f2c6b5cb6e78 36 fields · synced May 31, 2026