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Codan

FDA UDI

Class II (US FDA UDI)

by CODAN US Corporation

Identity

Trade Name
Codan FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
I.V. Set with Luer Lock FDA UDI
Model / Reference
B 403 FDA UDI
Description
I.V. Set with Luer Lock FDA UDI

Identifiers

Primary DI / UDI-DI
10813153020873 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive 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

No

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: Basic intravenous administration set, noninvasive

Codan by CODAN US Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CODAN US Corporation

Sources (1)

  • FDA UDI ec739fbb-2a06-4761-9134-a6db5fd57680 33 fields · synced May 30, 2026