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Infusomat®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Infusomat® FDA UDI
Generic Name
Bedside syringe pump FDA UDI
Device Name
INFUSOMAT SPACE - US VERSION ASSET FDA UDI
Model / Reference
8713050U-99 FDA UDI
Description
INFUSOMAT SPACE - US VERSION ASSET FDA UDI

Identifiers

Catalog Number
8713050U-99 FDA UDI
Primary DI / UDI-DI
04046964958274 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

Category: Bedside syringe pump

Infusomat® by B. Braun Medical 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

Sources (1)

  • FDA UDI 32be2ca1-c72f-4e98-85b1-9775f4978fb8 36 fields · synced May 30, 2026