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Atlanta BioMedical Model 4100

FDA UDI

Class II (US FDA UDI)

by Atlanta BioMedical Corporation

Identity

Trade Name
Atlanta BioMedical Model 4100 FDA UDI
Generic Name
Bedside syringe pump FDA UDI
Model / Reference
4100 FDA UDI

Identifiers

Catalog Number
4100 FDA UDI
Primary DI / UDI-DI
00863028000304 FDA UDI
510(k) Number
K072603 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Bedside syringe pump

Atlanta BioMedical Model 4100 by Atlanta BioMedical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedside syringe pump.

Cleared under the same submission

K072603 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atlanta BioMedical Corporation

Sources (1)

  • FDA UDI 6b7ac39c-bc1e-42c8-83be-4e1b77adf0a2 34 fields · synced May 30, 2026