Laboratorios Pisa S.A. De C.V.

Contact: Pamela Papineau
Web: http://www.pisa.com.mx
Address: Calle 7, N0. 1308 Zona Industrial, Guadalajara C.P. 44940, Mexico
Phone: +52-(133)-3678 1600 | Fax: +52-(133)-3812 9221 | Map/Directions >>

Profile: Laboratorios Pisa S.A. De C.V. specializes in the production of healthcare products. We offer products for areas such as anesthesiology & intensive care, hospital antibiotics, infection control, peritoneal dialysis, chronic diseases, clinic nutrition, prescription antibiotics, hemodialysis, ophthalmology, oncology, infusion therapy, pain therapy and for transplantation.

The company is ISO 9001:2000 certified.

FDA Registration Number: 3005440755
US Agent: Raza Mohammed / Pisa Biopharm Inc
Phone: +1-(518)-992-5944 E-Mail:

20 Products/Services (Click for related suppliers)

• Anesthesia Accessories

• Anesthesia Equipment

• Antibiotics

• Direct Patient Interface Nebulizer (FDA Code: CAF / 868.5630)

A nebulizer is a device intended to spray liquids in aerosol form into gases that are delivered directly to the patient for breathing. Heated, ultrasonic, gas, venturi, and refillable nebulizers are included in this generic type of device.

• Direct Patient Interface Respiratory Gas Humidifier (FDA Code: BTT / 868.5450)

A respiratory gas humidifier is a device that is intended to add moisture to, and sometimes to warm, the breathing gases for administration to a patient. Cascade, gas, heated, and prefilled humidifiers are included in this generic type of device.

• Immunoglobulin M (IgM) (FDA Code: DFT / 866.5550)

An immunoglobulin (light chain specific) immunological test system is a device that consists of the reagents used to measure by immunochemical techniques both kappa and lambda types of light chain portions of immunoglobulin molecules in serum, other body fluids, and tissues. In some disease states, an excess of light chains are produced by the antibody-forming cells. These free light chains, unassociated with gamma globulin molecules, can be found in a patient's body fluids and tissues. Measurement of the various amounts of the different types of light chains aids in the diagnosis of multiple myeloma (cancer of antibody-forming cells), lymphocytic neoplasms (cancer of lymphoid tissue), Waldenstrom's macroglobulinemia (increased production of large immunoglobulins), and connective tissue diseases such as rheumatoid arthritis or systemic lupus erythematosus.

• Infection Control Kits

• Infusion Systems

• Infusion Therapy Kits

• Injectable, Anesthesiology Products

• Latanoprost Ophthalmic Solution

• Liquid Hemodialysis Dialysate Concentrate Solution (FDA Code: KPO / 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.

• Nutritionals

• Oncology & Cancer Treatments

• Peritoneal Dialysis Sets

• Peritoneal Dialysis Units

• Tracheal Tube with/without Connector (FDA Code: BTR / 868.5730)

A tracheal tube is a device inserted into a patient's trachea via the nose or mouth and used to maintain an open airway.

• Tracheostomy Tube and Cuff (FDA Code: JOH / 868.5800)

A tracheostomy tube and tube cuff is a device intended to be placed into a surgical opening of the trachea to facilitate ventilation to the lungs. The cuff may be a separate or integral part of the tracheostomy tube and is, when inflated, intended to establish a seal between the tracheal wall and the tracheostomy tube. The cuff is used to prevent the patient's aspiration of substances, such as blood or vomit, or to provide a means for positive-pressure ventilation of the patient. This device is made of either stainless steel or plastic.

• Tracheostomy Tube with/without Connector (FDA Code: BTO / 868.5800)

• Transfusion Set