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Codan

FDA UDI

Class II (US FDA UDI)

by CODAN US Corporation

Identity

Trade Name
Codan FDA UDI
Generic Name
Non-absorbing intravenous administration set FDA UDI
Device Name
Trifurcated Extension Set; Colored Slide Clamps with Poly Ethylene Fluid Path FDA UDI
Model / Reference
BC 294 FDA UDI
Description
Trifurcated Extension Set; Colored Slide Clamps with Poly Ethylene Fluid Path FDA UDI

Identifiers

Primary DI / UDI-DI
10813153022747 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Non-absorbing intravenous administration 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

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: Non-absorbing intravenous administration set

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

Similar devices

Also classified as Non-absorbing intravenous administration set.

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 af375b6c-990e-48fd-b70c-a8763702ed70 33 fields · synced Jun 1, 2026