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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 infusion pump, single-channel FDA UDI
Device Name
Infusomat® Space® Large Volume Pump, Wireless FDA UDI
Model / Reference
8713051U FDA UDI
Description
Infusomat® Space® Large Volume Pump, Wireless FDA UDI

Identifiers

Catalog Number
8713051U FDA UDI
Primary DI / UDI-DI
04046964660887 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Bedside infusion pump, single-channel 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Bedside infusion pump, single-channel

Infusomat® by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedside infusion pump, single-channel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6e6cf6d4-e585-4be5-9d6e-131bf09de2ee 36 fields · synced Jun 8, 2026