Lifemed of California

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Contact: Patricia Brinker - VP QA & QC
Web: http://www.lifemedofcalifornia.com
E-Mail:
Address: 1216 So. Allec St., Anaheim, California 92805-6301, USA
Phone: +1-(714)-517-6900, 800-543-3633 | Fax: +1-(714)-517-6911 | Map/Directions >>

Profile: Lifemed of California is a manufacturer of medical devices. Our capabilities include integrated design development and production.

The company has revenues of USD 1-5 Million, has ~20 employees and is ISO 9001 certified.

FDA Registration Number: 2018692

8 Products/Services (Click for related suppliers)

• Anti-Regurgitation Valve with Blood Tubing Set (FDA Code: FJK / 876.5820)

A hemodialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and that consists of an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer.

• Cannula Clamp (FDA Code: FKC / 876.5540)

A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.

• I.V. Fluid Transfer Unit (FDA Code: LHI / 880.5440)

An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.

• Long-Term Indwelling Peritoneal Catheter (FDA Code: FJS / 876.5630)

(1) A peritoneal dialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions, and that consists of a peritoneal access device, an administration set for peritoneal dialysis, a source of dialysate, and, in some cases, a water purification mechanism. After the dialysate is instilled into the patient's peritoneal cavity, it is allowed to dwell there so that undesirable substances from the patient's blood pass through the lining membrane of the peritoneal cavity into this dialysate. These substances are then removed when the dialysate is drained from the patient. The peritoneal dialysis system may regulate and monitor the dialysate temperature, volume, and delivery rate together with the time course of each cycle of filling, dwell time, and draining of the peritoneal cavity or manual controls may be used. This generic device includes the semiautomatic and the automatic peritoneal delivery system.

• Product Design & Development

• Single-Use Medical Disposables

• Single-Use Peritoneal Dialysis Catheter (FDA Code: FKO / 876.5630)

• T-Type Infusion Blood Tubing Connector (FDA Code: FKB / 876.5820)