Liberty® PDx

FDA UDI

Class II (US FDA UDI)

by Fresenius Medical Care Holdings, Inc.

Identity

Trade Name: Liberty® PDx FDA UDI
Generic Name: Peritoneal dialysis system tubing set FDA UDI
Device Name: Liberty® PDx Cycler Set with Dual stay.safe® PIN Connectors FDA UDI
Model / Reference: 050-87220 FDA UDI
Description: Liberty® PDx Cycler Set with Dual stay.safe® PIN Connectors FDA UDI

Identifiers

Catalog Number: 050-87220 FDA UDI
Primary DI / UDI-DI: 00840861101979 FDA UDI
FDA Product Code: FKX FDA UDI
GMDN Term: Peritoneal dialysis system tubing set FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5630 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Peritoneal dialysis system tubing set

Liberty® PDx by Fresenius Medical Care Holdings, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Fresenius Medical Care Holdings, Inc.

Sources (1)

FDA UDI 0a4a4264-e05d-433a-adfc-4cd7eaf37e60 35 fields · synced Jun 8, 2026