Skype

Jedmed Instrument Company

Click Here To EMAIL INQUIRY
Web: http://www.jedmed.com
E-Mail:
Address: 5416 JEDMED Court, St. Louis, Missouri 63129-2221, USA
Phone: +1-(314)-845-3770 | Fax: +1-(314)-845-3771 | Map/Directions >>
 
 

Profile: Jedmed Instrument Company manufactures instruments in the areas of ENT, opthalmology and dentistry. Our endonasal DCR technique uses a fiberoptic probe inserted in the punctum for guidance. Our kaps tri-gem microscope utilizes a quartz-halogen fiberoptic illumination system. The source is mounted on the microscope arm allowing the fiberoptic cable to be shorter. This combination enables the maximum of light to be transmitted to the field.

The company has revenues of < USD 1 Million, has ~40 employees and is ISO certified.

FDA Registration Number: 1926681

201 to 250 of 336 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 2 3 4 [5] 6 7 >> Next 50 Results
• Nasal Speculums
• Nasal Speculums
• 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.
• Needle Pulling Tissue Forceps
• Neurosurgical Head Rest (FDA Code: HBM / 882.4440)
A neurosurgical headrest is a device used to support the patient's head during a surgical procedure.
• Non Rigid Laryngoscope (FDA Code: CAL / 868.5530)
A flexible laryngoscope is a fiberoptic device used to examine and visualize a patient's upper airway and aid placement of a tracheal tube.
• Non-Powered Ophthalmic Instrument Stand (FDA Code: HMG / 886.1860)
An ophthalmic instrument stand is an AC-powered or nonpowered device intended to store ophthalmic instruments in a readily accessible position.
• Non-Sterile Prosthesis Modification For Ossicular Replacement Surgery Instrument (FDA Code: NNS / 874.3540)
A prosthesis modification instrument for ossicular replacement surgery is a device intended for use by a surgeon to construct ossicular replacements. This generic type of device includes the ear, nose, and throat cutting block; wire crimper, wire bending die; wire closure forceps; piston cutting jib; gelfoamTMpunch; wire cutting scissors; and ossicular finger vise.
• Non-Surgical Tongue Depressor (FDA Code: FMA / 880.6230)
A tongue depressor is a device intended to displace the tongue to facilitate examination of the surrounding organs and tissues.
• 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.
• Occlusive Wound Dressing (FDA Code: NAD / 878.4020)
An occlusive wound dressing is a nonresorbable, sterile or non-sterile device intended to cover a wound, to provide or support a moist wound environment, and to allow the exchange of gases such as oxygen and water vapor through the device. It consists of a piece of synthetic polymeric material, such as polyurethane, with or without an adhesive backing. This classification does not include an occlusive wound dressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.
• Ocular Pressure Applicator (FDA Code: LCC / 886.4610)
An ocular pressure applicator is a manual device that consists of a sphygmomanometer-type squeeze bulb, a dial indicator, a band, and bellows, intended to apply pressure on the eye in preparation for ophthalmic surgery.
• Open valve nasal speculum
• Operating Room Television Monitor
• Ophthalmic Aspiration Cannula (FDA Code: HMX / 886.4350)
A manual ophthalmic surgical instrument is a nonpowered, handheld device intended to aid or perform ophthalmic surgical procedures. This generic type of device includes the manual corneal burr, ophthalmic caliper, ophthalmic cannula, eyelid clamp, ophthalmic muscle clamp, iris retractor clip, orbital compressor, ophthalmic curette, cystotome, orbital depressor, lachrymal dilator, erisophake, expressor, ophthalmic forcep, ophthalmic hook, sphere introducer, ophthalmic knife, ophthalmic suturing needle, lachrymal probe, trabeculotomy probe, cornea-sclera punch, ophthalmic retractor, ophthalmic ring (Flieringa), lachrymal sac rongeur, ophthalmic scissors, enucleating snare, ophthalmic spatula, ophthalmic specula, ophthalmic spoon, ophthalmic spud, trabeculotome or ophthalmic manual trephine.
• Ophthalmic Cannula (FDA Code: HMX / 886.4350)
• 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 Forceps (FDA Code: HNR / 886.4350)
• Ophthalmic Headband Mirror (FDA Code: HKF / 886.1500)
A headband mirror is a device intended to be strapped to the head of the user to reflect light for use in examination of the eye.
• Ophthalmic Instrument Stand (FDA Code: HMG / 886.1860)
• Ophthalmic Manual Trephine (FDA Code: HRH / 886.4350)
• Ophthalmic Needles
• Ophthalmic Operating Spectacle (FDA Code: HOH / 886.4770)
Ophthalmic operating spectacles (loupes) are devices that consist of convex lenses or lens systems intended to be worn by a surgeon to magnify the surgical site during ophthalmic surgery.
• 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.
• Ophthalmic Probe
• Ophthalmic Retractor (FDA Code: HNI / 886.4350)
• Ophthalmic Spatula (FDA Code: HND / 886.4350)
• Ophthalmic Speculum (FDA Code: HNC / 886.4350)
• Ophthalmic Sponge (FDA Code: HOZ / 886.4790)
An ophthalmic sponge is a device that is an absorbant sponge, pad, or spear made of folded gauze, cotton, cellulose, or other material intended to absorb fluids from the operative field in ophthalmic surgery.
• Ophthalmic Suture Scissors (FDA Code: HNF / 886.4350)
• Ophthalmic Suturring Needle (FDA Code: HNM / 886.4350)
• Ophthalmic Tenotomy Scissors
• Ophthalmology, Surgical Instrument Trays
• Orthopedic Osteotome (FDA Code: HWM / 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.
• Otoscopes
• Otoscopes (FDA Code: ERA / 874.4770)
An otoscope is a device intended to allow inspection of the external ear canal and tympanic membrane under magnification. The device provides illumination of the ear canal for observation by using an AC- or battery-powered light source and an optical magnifying system.
• Over-the-Ear Cannulas
• Partial Ossicular Replacement Prosthesis (FDA Code: ETB / 874.3450)
A partial ossicular replacement prosthesis is a device intended to be implanted for the functional reconstruction of segments of the ossicular chain and facilitates the conduction of sound wave from the tympanic membrane to the inner ear. The device is made of materials such as stainless steel, tantalum, polytetrafluoroethylene, polyethylene, polytetrafluoroethylene with carbon fibers composite, absorbable gelatin material, porous polyethylene, or from a combination of these materials.
• Patient Transfer Chair
• Photokeratoscope (FDA Code: HJA / 886.1350)
A keratoscope is an AC-powered or battery-powered device intended to measure and evaluate the corneal curvature of the eye. Lines and circles within the keratoscope are used to observe the corneal reflex. This generic type of device includes the photokeratoscope which records corneal curvature by taking photographs of the cornea.
• Plastic Hemostatic Forceps
• Plastic Surgery Scissors
• Platinum Lid Chain
• Porous Polyethylene Ossicular Prosthesis (FDA Code: LBM / 874.3450)
• Porous Polyethylene Total Ossicular Prosthesis (FDA Code: LBN / 874.3495)
A total ossicular replacement prosthesis is a device intended to be implanted for the total functional reconstruction of the ossicular chain and facilitates the conduction of sound waves from the tympanic membrance to the inner ear. The device is made of materials such as polytetrafluoroethylene, polytetrafluoroethylene with vitreous carbon fibers composite, porous polyethylene, or from a combination of these materials.
• Powered Nasal Irrigator (FDA Code: KMA / 874.5550)
A powered nasal irrigator is an AC-powered device intended to wash the nasal cavity by means of a pressure-controlled pulsating stream of water. The device consists of a control unit and pump connected to a spray tube and nozzle.
• Radiographic Film Illuminator (FDA Code: IXC / 892.1890)
A radiographic film illuminator is a device containing a visible light source covered with a translucent front that is intended to be used to view medical radiographs.
• Ragnell Retractor
• Rasps

 Edit or Enhance this Company (4075 potential buyers viewed listing,  631 forwarded to manufacturer's website)
Browse Category   |   Alphabetical Products   |   ALL 25,000 Suppliers
HomeBuyAdd FREE ListingAdvertise Medical CompanyMedical Portal