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Micromedics, Inc.

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Contact: Mr. Kevin Connelly - Sales Manager
Web: http://www.micromedics.com
E-Mail:
Address: 1270 Eagan Industrial Rd., St. Paul, Minnesota 55121-1385, USA
Phone: +1-(651)-452-1977 | Fax: +1-(651)-452-1787 | Map/Directions >>
 
 

Profile: Micromedics, Inc. manufactures, develops, and markets various proprietary medical products. Our product list comprises of implants & instruments for ear, nose & throat (ENT) surgery, products for organizing & protecting surgical instruments, applicators for biomaterials, and ear care products. Our FibriJet® biomaterials applicators consist of specially designed dual-syringe applicators with procedure-specific tips. They are used to apply biomaterials such as fibrin tissue sealant and concentrated plasma gel. DizzyFIX™ is our FDA cleared device for the treatment of vertigo.

The company was founded in 1982, has revenues of USD 5-10 Million, has ~70 employees and is ISO 9001,CE certified.

FDA Registration Number: 2183425

34 Products/Services (Click for related suppliers)  
• Applicator
• Arthroscopy Instruments
• Autoclave Systems
• Catheter Accessories (FDA Code: KGZ / 878.4200)
An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities, or evaluate certain physiologic conditions. Examples include irrigation and drainage catheters, pediatric catheters, peritoneal catheters (including dialysis), and other general surgical catheters. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. Examples of accessories include adaptors, connectors, and catheter needles.
• 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.
• Disposable Surgical Instrument (FDA Code: KDC / 878.4800)
A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.
• Ear Implants
• Ear Popper
• Ear Speculum (FDA Code: EPY / 878.1800)
A speculum is a device intended to be inserted into a body cavity to aid observation. It is either nonilluminated or illuminated and may have various accessories.
• Ear Wick (FDA Code: KCN / 874.5220)
An ear, nose, and throat drug administration device is one of a group of ear, nose, and throat devices intended specifically to administer medicinal substances to treat ear, nose, and throat disorders. These instruments include the powder blower, dropper, ear wick, manual nebulizer pump, and nasal inhaler.
• Endoscopes Tray
• Epistaxis Balloon (FDA Code: EMX / 874.4100)
An epistaxis balloon is a device consisting of an inflatable balloon intended to control internal nasal bleeding by exerting pressure against the sphenopalatine artery.
• General & Plastic Surgery Laparoscope (FDA Code: GCJ / 876.1500)
An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
• Instruments For Arthroscopy
• Intranasal Septal Splint (FDA Code: LYA / 874.4780)
An intranasal splint is intended to minimize bleeding and edema and to prevent adhesions between the septum and the nasal cavity. It is placed in the nasal cavity after surgery or trauma. The intranasal splint is constructed from plastic, silicone, or absorbent material.
• Microsurgical Ear Pick (FDA Code: JYT / 874.4420)
• Middle Ear Inflation Device (FDA Code: MJV)
• Myringotomy Blades & Knives
• Myringotomy Instruments
• Myringotomy Knife (FDA Code: JYP / 874.4420)
• Nasal Septal Button (FDA Code: LFB)
• Nasal Splints (FDA Code: EPP / 874.5800)
An external nasal splint is a rigid or partially rigid device intended for use externally for immobilization of parts of the nose.
• Non Dental Irrigating Syringe (FDA Code: KYZ / 880.6960)
An irrigating syringe is a device intended for medical purposes that consists of a bulb or a piston syringe with an integral or a detachable tube. The device is used to irrigate, withdraw fluid from, or instill fluid into, a body cavity or wound.
• Nose And Throat Ear Bur (FDA Code: EQJ / 874.4140)
An ear, nose, and throat bur is a device consisting of an interchangeable drill bit that is intended for use in an ear, nose, and throat electric or pneumatic surgical drill (874.4250) for incising or removing bone in the ear, nose, or throat area. The bur consists of a carbide cutting tip on a metal shank or a coating of diamond on a metal shank. The device is used in mastoid surgery, frontal sinus surgery, and surgery of the facial nerves.
• Ophthalmology Instruments
• 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.
• Silicone Elastomer (FDA Code: MDA / 878.4025)
• Silicone Sheeting
• Sinoscopy Instruments
• Sinus Cannula (FDA Code: KAM / 878.4800)
• Soft Ear Speculum (FDA Code: EPY / 878.1800)
• Sterilization Wrap Containers (FDA Code: KCT / 880.6850)
A sterilization wrap (pack, sterilization wrapper, bag, or accessories, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used.
• Surgical Instrument Tray (FDA Code: FSM / 878.4800)
• Tympanostomy Tube (FDA Code: ETD / 874.3880)
A tympanostomy tube is a device that is intended to be implanted for ventilation or drainage of the middle ear. The device is inserted through the tympanic membrane to permit a free exchange of air between the outer ear and middle ear. A type of tympanostomy tube known as the malleous clip tube attaches to the malleous to provide middle ear ventilation. The device is made of materials such as polytetrafluoroethylene, polyethylene, silicon elastomer, or porous polyethylene.

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