Lifemed Lifecoil Chronic Peritoneal Catheter

FDA UDI

Class II (US FDA UDI)

by Lifemed of California

Identity

Trade Name: Lifemed Lifecoil Chronic Peritoneal Catheter FDA UDI
Generic Name: Peritoneal dialysis catheter, chronic FDA UDI
Device Name: Lifecoil Chronic Peritoneal Catheter with Radiopaque Stripe and Two Attached Cuffs FDA UDI
Model / Reference: PD6101 FDA UDI
Description: Lifecoil Chronic Peritoneal Catheter with Radiopaque Stripe and Two Attached Cuffs FDA UDI

Identifiers

Catalog Number: PD6101 FDA UDI
Primary DI / UDI-DI: 00852250006024 FDA UDI
FDA Product Code: FKX FDA UDI
GMDN Term: Peritoneal dialysis catheter, chronic 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

Yes

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

Dimensions & Sizes

Size: Length — 62 Centimeter FDA UDI
Outer Diameter — 4.69 Millimeter FDA UDI
Lumen/Inner Diameter — 2.66 Millimeter FDA UDI

Category: Peritoneal dialysis catheter, chronic

Lifemed Lifecoil Chronic Peritoneal Catheter by Lifemed of California — 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: Lifemed of California

Sources (1)

FDA UDI b3c70ea3-3b80-49fe-a71a-7eaa671c176c 37 fields · synced May 29, 2026