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Fresenius Kabi

FDA UDI

Class II (US FDA UDI)

by CODAN US Corporation

Identity

Trade Name
FRESENIUS KABI FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
SHORT EXTENSION SET FDA UDI
Model / Reference
FK20203KE FDA UDI
Description
SHORT EXTENSION SET FDA UDI

Identifiers

Primary DI / UDI-DI
10813153027520 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Intravenous administration tubing extension 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

Yes

FDA UDI

Category: Intravenous administration tubing extension set

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

Similar devices

Also classified as Intravenous administration tubing extension 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 46df2b56-5f59-4f4a-a78f-fca0af80f0f9 33 fields · synced Jun 1, 2026