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Introcan Safety ® 2

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Introcan Safety ® 2 FDA UDI
Generic Name
Peripheral vascular intervention infusion catheter FDA UDI
Device Name
Introcan Safety 2 - 24G x 0.75 in., PUR, Winged FDA UDI
Model / Reference
4232003-02 FDA UDI
Description
Introcan Safety 2 - 24G x 0.75 in., PUR, Winged FDA UDI

Identifiers

Catalog Number
4232003-02 FDA UDI
Primary DI / UDI-DI
04046955341832 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral vascular intervention infusion catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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
MRI Safety
MR Conditional FDA UDI

Category: Peripheral vascular intervention infusion catheter

Introcan Safety ® 2 by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular intervention infusion catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7989ea6e-ca61-4d22-82a6-fba0feb81a17 36 fields · synced May 30, 2026