Profile: 3M Medical Specialties and OEM Products offers solutions, technologies and services for health care product development. We produce a wide range of medical tapes, diagnostic components and optical supplies. We also offer OEM procedure tray products and medical sterilization specialties. Our 3M™ polyester diagnostic tape 9794R is a hydrophobic acrylic adhesive coated on optically clear polyester film, high strength film designed for rigidity & durability of finished device & provided on a white paper release liner. Our optical products are recognized by optical laboratories around the world to assist in the manufacturing of prescription optics. Our Hi-Performance STS Polyethylene, 4.4 mil double coated tape 1517, 58# is a highly conformable double coated medical tape consisting of a 1 mil polyethylene backing. It provides excellent adhesion to most medical device substrates.

FDA Registration Number: 1717046

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• Ortho Splints Walkers

• Orthopedic Surgical Drapes

• Orthoplast Splints For Hummers

• Orthoses, Humeral Splints

• Overhead Supported Arm Sling (FDA Code: ILE / 890.3475) A limb orthosis (brace) is a device intended for medical purposes that is worn on the upper or lower extremities to support, to correct, or to prevent deformities or to align body structures for functional improvement. Examples of limb orthoses include the following: A whole limb and joint brace, a hand splint, an elastic stocking, a knee cage, and a corrective shoe.

• Oxygen Aids

• Pediatric Monitoring Electrodes

• Perforated Adhesive Cloth

• Permacel Adhesive Cloth

• Phonocardiograph (FDA Code: DQC / 870.2390) A phonocardiograph is a device used to amplify or condition the signal from a heart sound transducer. This device furnishes the excitation energy for the transducer and provides a visual or audible display of the heart sounds.

• Physical/Chemical Sterilization Process Indicator (FDA Code: JOJ / 880.2800) A biological sterilization process indicator is a device intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor adequacy of sterilization. The device consists of a known number of microorganisms, of known resistance to the mode of sterilization, in or on a carrier and enclosed in a protective package. Subsequent growth or failure of the microorganisms to grow under suitable conditions indicates the adequacy of sterilization.

• Prefabricated thumb splints

• Programmable Autoclaves

• Protective Disposable Garments

• Protective Padding & Dressings

• Protective Wear

• Radiographic Film (FDA Code: IWZ / 892.1840) Radiographic film is a device that consists of a thin sheet of radiotransparent material coated on one or both sides with a photographic emulsion intended to record images during diagnostic radiologic procedures.

• Radiological Digital Image Communication System (FDA Code: LMD / 892.2020) A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, interfaces, and a communications protocol.

• Radiological Image Processing System (FDA Code: LLZ / 892.2050) A picture archiving and communications system is a device that provides one or more capabilities relating to the acceptance, transfer, display, storage, and digital processing of medical images. Its hardware components may include workstations, digitizers, communications devices, computers, video monitors, magnetic, optical disk, or other digital data storage devices, and hardcopy devices. The software components may provide functions for performing operations related to image manipulation, enhancement, compression or quantification.

• Reagent/Device, Inoculum Calibration (FDA Code: LIE / 866.1640) An antimicrobial susceptibility test powder is a device that consists of an antimicrobial drug powder packaged in vials in specified amounts and intended for use in clinical laboratories for determining in vitro susceptibility of bacterial pathogens to these therapeutic agents. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases.

• Reinforced Skin Closures

• Reloadable Linear Staplers

• Removable Skin Staple (FDA Code: GDT / 878.4760) A removable skin staple is a staple-like device intended to connect external tissues temporarily to aid healing. It is not absorbable.

• Resting Monitoring EKG Electrodes

• Reusable Hot /Cold Pack (FDA Code: IME / 890.5700) A cold pack is a device intended for medical purposes that consists of a compact fabric envelope containing a specially hydrated pliable silicate gel capable of forming to the contour of the body and that provides cold therapy for body surfaces.

• Reusable Skin Stapler

• Roticulating Staplers

• Roticulating Staplers with Absorbable Staples

• Roticulating Staplers with Titanium Staples

• Roticulating Staplers, Single Use Instrument

• Rubber Elastic Bandages

• Self Adhesive Elastic Bandage

• Self-Adherent Wraps/Bandages

• Self-Adhesive Cloth

• Shin Splints

• Shoes & Boots

• Single Use Skin Staple Remover

• Single-Use Clinical Thermometers

• Skin Closures

• Skin Closures, Knee Braces

• Skin Closures, Passive Closure Devices

• Skin Closures, Skin Staplers

• Skin Creams & Lotions

• Skin Fascia Stapler

• Skin Pressure Protector (FDA Code: FMP / 880.6450) A skin pressure protector is a device intended for medical purposes that is used to reduce pressure on the skin over a bony prominence to reduce the likelihood of the patient's developing decubitus ulcers (bedsores).

• Skin Protectant Liquid Bandage (FDA Code: NEC / 880.5090) A liquid bandage is a sterile device that is a liquid, semiliquid, or powder and liquid combination used to cover an opening in the skin or as a dressing for burns. The device is also used as a topical skin protectant.

• Skin Staplers

• Skin Staplers & Removers

• Skin Staplers with Stainless Steel Staples)

• Soap & Soap Dispensers