Profile: Halyard Health, Inc. is a consumer & medical products company. Its global tissue, personal care and health care brands include Huggies, Pull-Ups, Kotex, Depend, Kleenex, Scott, Kimwipes and WypAll. Our product lines include closed suction systems, oral care, gastric lavage, multifunction electrodes, pain management, medical gloves, facial protection, gastrointestinal Endoscopy, enternal feeding tubes, closed suction systems, cardiac multifunction electrodes enteral feeding, endoscopy and diagnostics, as well as device accessories. The gastric lavage systems rapidly and effectively cleanse the stomachs of patients suffering from accidental poisoning, drug overdoses or gastrointestinal bleeding.

The company was founded in 1903, has revenues of > USD 1 Billion, has ~30 employees and is CE certified.

FDA Registration Number: 3011270181

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• MRI Safe Blood Pressure Cuff

• Nasal Endotracheal Tubes

• Natural Face Masks

• Neonatal Disposable Blood Pressure Cuffs

• New Or Used Disposable Examination Gowns and Capes

• Non-Cantilevered Ringed Forceps

• Non-Conductive Shoe Cover

• Non-reinforced Surgical Gowns

• Non-Surgical Isolation Gown (FDA Code: OEA / 878.4040) Surgical apparel are devices that are intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from transfer of microorganisms, body fluids, and particulate material. Examples include surgical caps, hoods, masks, gowns, operating room shoes and shoe covers, and isolation masks and gowns. Surgical suits and dresses, commonly known as scrub suits, are excluded.

• Nursing Caps

• Nursing Gowns

• Nursing Scrubs

• Obstetrical Forceps (FDA Code: HDA / 884.4400) An obstetric forceps is a device consisting of two blades, with handles, designed to grasp and apply traction to the fetal head in the birth passage and facilitate delivery.

• Open Biopsy Forceps

• Open Cuff Silicone Face Masks

• Operating Room Sheet

• Operating Room Shoe Cover (FDA Code: FXP / 878.4040)

• Ophthalmic Epilation Forceps

• Ophthalmic Eye Shield (FDA Code: HOY / 886.4750) An ophthalmic eye shield is a device that consists of a plastic or aluminum eye covering intended to protect the eye or retain dressing materials in place.

• Ophthalmic Patient Drape (FDA Code: HMT / 878.4370) A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as to isolate a site of surgical incision from microbial and other contamination. The device includes a plastic wound protector that may adhere to the skin around a surgical incision or be placed in a wound to cover its exposed edges, and a latex drape with a self-retaining finger cot that is intended to allow repeated insertion of the surgeon's finger into the rectum during performance of a transurethral prostatectomy.

• Oral Endotracheal Tubes

• Ortho Splints Walkers

• Orthopedic Fixation Accessories (FDA Code: LYT / 888.3030) Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.

• Orthopedic Forceps

• Orthoplast Splints For Hummers

• Orthoses, Humeral Splints

• OSHA Compliant, Caps

• OSHA Compliant, Protective Disposable Garments

• OSHA Compliant, Protective Gowns

• Oval Cupped Intraocular Forceps

• Ovarian Biopsy Forceps

• Paper Face Masks

• Paracentesis Cannulas

• Paracentesis Needle

• Paracentesis Trays & Kits

• Patient Apparel Products

• Patient Examination Gowns & Capes

• Patient Examination Gowns and Capes (FDA Code: FME / 880.6265) An examination gown is a device intended for medical purposes that is made of cloth, paper, or other material that is draped over or worn by a patient as a body covering during a medical examination.

• Pediatric Diaper

• Pediatric Endotracheal Tubes

• Pediatric Garments

• Pediatric Multifunction Electrodes

• PEG Feeding Tubes/Kits

• 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.

• plastic Forceps

• Poly Patient Examination Glove (FDA Code: LZA / 880.6250) A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.

• Polyglycolic Acid Synthetic Absorbable Suture (FDA Code: GAM / 878.4493) An absorbable poly(glycolide/l-lactide) surgical suture (PGL suture) is an absorbable sterile, flexible strand as prepared and synthesized from homopolymers of glycolide and copolymers made from 90 percent glycolide and 10 percentl-lactide, and is indicated for use in soft tissue approximation. A PGL suture meets United States Pharmacopeia (U.S.P.) requirements as described in the U.S.P. "Monograph for Absorbable Surgical Sutures;" it may be monofilament or multifilament (braided) in form; it may be uncoated or coated; and it may be undyed or dyed with an FDA-approved color additive. Also, the suture may be provided with or without a standard needle attached.

• Polytetrafluoroethylene Vitreous Carbon Material for Maxillofacial Reconstruction (FDA Code: KKY / 878.3500) A polytetrafluoroethylene with carbon fibers composite implant material is a porous device material intended to be implanted during surgery of the chin, jaw, nose, or bones or tissue near the eye or ear. The device material serves as a space-occupying substance and is shaped and formed by the surgeon to conform to the patient's need.

• Post-Surgery Compression Garments

• Postsurgical Garments