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BD® Alaris™ Syringe Module, Model 8110

FDA UDI

Class II (US FDA UDI)

by CareFusion 303, INC

Identity

Trade Name
BD® Alaris™ Syringe Module, Model 8110 FDA UDI
Generic Name
Bedside syringe pump FDA UDI
Device Name
BD Alaris™ Syringe Module, Model 8110 v12.3.0 FDA UDI
Model / Reference
8110 FDA UDI
Description
BD Alaris™ Syringe Module, Model 8110 v12.3.0 FDA UDI

Identifiers

Catalog Number
8110BDADXEN123 FDA UDI
Primary DI / UDI-DI
10885403516047 FDA UDI
FDA Product Code
FRN 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

BD® Alaris™ Syringe Module, Model 8110 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 6c4c9dc2-e0b8-401e-8d2d-5f472098ad56 36 fields · synced May 30, 2026