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Outlook®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Outlook® FDA UDI
Generic Name
Bedside infusion pump, single-channel FDA UDI
Device Name
CONVERSION 100ES TO 400ES FDA UDI
Model / Reference
621-124ES FDA UDI
Description
CONVERSION 100ES TO 400ES FDA UDI

Identifiers

Catalog Number
621-124ES FDA UDI
Primary DI / UDI-DI
04046964336614 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bedside infusion pump, single-channel

Outlook® 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

Manufacturer
B. Braun Medical Inc.

Sources (1)

  • FDA UDI c1c5bfa1-46ef-4d61-8f6b-073fc53db2ab 36 fields · synced Jun 8, 2026