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IV Administration Set

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
IV Administration Set FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
TRANSFER SET 24 IN. FDA UDI
Model / Reference
480202 FDA UDI
Description
TRANSFER SET 24 IN. FDA UDI

Identifiers

Catalog Number
480202 FDA UDI
Primary DI / UDI-DI
04046955050147 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Fluid transfer set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluid transfer set, general-purpose

IV Administration Set by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluid transfer set, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI db51415e-d65a-46f3-a03f-01b819f513c4 35 fields · synced May 30, 2026