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Liberty® Select Cycler

FDA UDI

Class II (US FDA UDI)

by Fresenius Medical Care Holdings, Inc.

Identity

Trade Name
Liberty® Select Cycler FDA UDI
Generic Name
Peritoneal dialysis system FDA UDI
Device Name
Liberty® Select Cycler FDA UDI
Model / Reference
180343 FDA UDI
Description
Liberty® Select Cycler FDA UDI

Identifiers

Primary DI / UDI-DI
00840861102068 FDA UDI
510(k) Number
K171652 FDA UDI
K181108 FDA UDI
K222318 FDA UDI
FDA Product Code
FKX FDA UDI
GMDN Term
Peritoneal dialysis system 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 32 Pound FDA UDI

Category: Peritoneal dialysis system

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

Similar devices

Also classified as Peritoneal dialysis system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b6169658-7d4b-43b3-a5ad-4f8c3822ccef 36 fields · synced May 30, 2026