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Liberty

FDA UDI

Class II (US FDA UDI)

by Fresenius Medical Care Renal Therapies Group, LLC

Identity

Trade Name
Liberty FDA UDI
Generic Name
Peritoneal dialysis system tubing set FDA UDI
Device Name
Liberty Cycler Set, single stay•safe® PIN patient connector, 10-foot patient line, 30-inch drain line FDA UDI
Model / Reference
050-87215A FDA UDI
Description
Liberty Cycler Set, single stay•safe® PIN patient connector, 10-foot patient line, 30-inch drain line FDA UDI

Identifiers

Primary DI / UDI-DI
00840861102709 FDA UDI
510(k) Number
K173718 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

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

Category: Peritoneal dialysis system tubing set

Liberty by Fresenius Medical Care Renal Therapies Group, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peritoneal dialysis system tubing set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7d350dc7-64f5-4d2d-af8b-ebdc9d6daa54 35 fields · synced Jun 8, 2026