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B.braun

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
B.BRAUN FDA UDI
Generic Name
Medication transfer set FDA UDI
Device Name
Intermittent Injection Port with 19 Ga. x 1 in. Needle FDA UDI
Model / Reference
418019 FDA UDI
Description
Intermittent Injection Port with 19 Ga. x 1 in. Needle FDA UDI

Identifiers

Catalog Number
418019 FDA UDI
Primary DI / UDI-DI
04022495769961 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Medication transfer set 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: Medication transfer set

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

Similar devices

Also classified as Medication transfer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dae0ded8-d6bd-4cad-a0c7-41a1ccc2aff9 36 fields · synced May 30, 2026