Procedure Products, Inc.

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Web: http://www.procedureproducts.com
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Address: 6622 SE Oakridge Drive, Gladstone, Oregon 97027, USA
Phone: +1-(360)-693-1832 | Fax: +1-(360)-690-4473 | Map/Directions >>

Profile: Procedure Products, Inc. manufactures numerous hospital special-procedure needles. We also produce our signature non-glare color-coded syringes and special control syringes in a wide variety of sizes and colors. Our guide-wire torque devices, waste fluid systems, adapters and high pressure connectors are specifically designed for radiology and cardiology. We are capable of manufacturing additional varieties of drug labeled syringes.

The company was founded in 1985, has revenues of USD 1-5 Million.

FDA Registration Number: 3020778

28 Products/Services (Click for related suppliers)

• Angiography Palm Pad Syringes

• Aspiration Cytology Biopsy Needles

• Aspiration Syringe

• Autoclavable Bowls

• Cardiac Catherization Needles

• Cardiopulmonary Bypass Adaptor (FDA Code: DTL / 870.4290)

A cardiopulmonary bypass adaptor, stopcock, manifold, or fitting is a device used in cardiovascular diagnostic, surgical, and therapeutic applications to interconnect tubing, catheters, or other devices.

• Color Coded Autoclavable semi-clear Medicine Cups

• Color coded Control Syringes

• Cytology Cervical Spatula (FDA Code: HHT / 884.4530)

An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

• Diagnostic Intravascular Catheter (FDA Code: DQO / 870.1200)

An intravascular diagnostic catheter is a device used to record intracardiac pressures, to sample blood, and to introduce substances into the heart and vessels. Included in this generic device are right-heart catheters, left-heart catheters, and angiographic catheters, among others.

• Fixed High Pressure Connectors

• Guidewire Catheter (FDA Code: DQX / 870.1330)

A catheter guide wire is a coiled wire that is designed to fit inside a percutaneous catheter for the purpose of directing the catheter through a blood vessel.

• I.V. Container (FDA Code: KPE / 880.5025)

An I.V. container is a container made of plastic or glass used to hold a fluid mixture to be administered to a patient through an intravascular administration set.

• Intravenous Administration Kit (FDA Code: FPA / 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.

• Laparoscopic Insufflator (FDA Code: HIF / 884.1730)

A laparoscopic insufflator is a device used to facilitate the use of the laparoscope by filling the peritoneal cavity with gas to distend it.

• Needle Disposal Boxes

• Percutaneous Catheterization Vessel Dilator (FDA Code: DRE / 870.1310)

A vessel dilator for percutaneous catheterization is a device which is placed over the guide wire to enlarge the opening in the vessel, and which is then removed before sliding the catheter over the guide wire.

• Piston Syringe (FDA Code: FMF / 880.5860)

A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.

• Potts Cournand Needles

• Pressure Monitoring Lines

• Scalpel Disposal Boxes

• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570)

A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.

• Stopcock, I.V.Set (FDA Code: FMG / 880.5440)

• Swivel High Pressure Connectors

• Syringe Injection Lines

• Syringe Needle Introducer (FDA Code: KZH / 880.6920)

A syringe needle introducer is a device that uses a spring-loaded mechanism to drive a hypodermic needle into a patient to a predetermined depth below the skin surface.

• Torque Adapters

• Waste Bags