Elcon Medical Instruments GmbH

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Contact: Mr. Holger Lücke - Managing Director
Web: http://www.elcon-medical.com
E-Mail:
Address: Dr. Karl-Storz-Straße 26, Tuttlingen D-78532, Germany
Phone: +49-(7461)-9281-0 | Fax: +49-(7461)-9281-29 | Map/Directions >>
 
 

Profile: Elcon Medical Instruments GmbH is a manufacturer and distributor of surgical instruments. Our wide range of instruments cover all surgical disciplines. We offer instruments for general surgery, gynecology, ENT surgery, cardiovascular surgery, neuro, ophthalmology, facial surgery and laparoscopy.

The company is ISO 13485:2003 certified.

FDA Registration Number: 8043816
US Agent: Dagmar Maser / Business Support International
Phone: +1-(212)-331-8358  Fax: +1-(212)-257-6441  E-Mail:

1 to 50 of 76 Products/Services (Click for related suppliers)  Page: [1] 2 >> Next 50 Results
• AC-Powered Motor Orthopedic Surgical Instrument (FDA Code: HWE / 878.4820)
Surgical instrument motors and accessories are AC-powered, battery-powered, or air-powered devices intended for use during surgical procedures to provide power to operate various accessories or attachments to cut hard tissue or bone and soft tissue. Accessories or attachments may include a bur, chisel (osteotome), dermabrasion brush, dermatome, drill bit, hammerhead, pin driver, and saw blade.
• Adenoid Curettes (FDA Code: KBJ / 874.4420)
• Adenotomes (FDA Code: KBH / 874.4420)
• Cardiovascular Biopsy Needle (FDA Code: DWO / 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.
• Cardiovascular Surgical Instrument (FDA Code: DWS / 870.4500)
Cardiovascular surgical instruments are surgical instruments that have special features for use in cardiovascular surgery. These devices include, e.g., forceps, retractors, and scissors.
• Chisel/Osteotome (FDA Code: KDG / 878.4820)
• Disconnect Forceps (FDA Code: FJR / 876.5540)
A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.
• Disposable Medical Scissors (FDA Code: JOK / 880.6820)
Medical disposable scissors are disposable type general cutting devices intended for medical purposes. This generic type of device does not include surgical scissors.
• 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.
• Elastic Bandages (FDA Code: FQM / 880.5075)
An elastic bandage is a device consisting of either a long flat strip or a tube of elasticized material that is used to support and compress a part of a patient's body.
• Emesis Basin (FDA Code: FNY / 880.6730)
A body waste receptacle is a device intended for medical purposes that is not attached to the body and that is used to collect the body wastes of a bed patient.
• ENT Forceps (FDA Code: KAE / 874.4420)
• ENT Nasal Gouge (FDA Code: KAQ / 874.4420)
• Episiotomy Scissors (FDA Code: HDK / 884.4520)
An obstetric-gynecologic general manual instrument is one of a group of devices used to perform simple obstetric and gynecologic manipulative functions. This generic type of device consists of the following:
• Fixed Size Cervical Dilator (FDA Code: HDQ / 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:
• Forceps (FDA Code: HTD / 878.4800)
• Gastro-Urology Probe and Director (FDA Code: FGM / 876.4730)
A manual gastroenterology-urology surgical instrument and accessories is a device designed to be used for gastroenterological and urological surgical procedures. The device may be nonpowered, hand-held, or hand-manipulated. Manual gastroenterology-urology surgical instruments include the biopsy forceps cover, biopsy tray without biopsy instruments, line clamp, nonpowered rectal probe, nonelectrical clamp, colostomy spur-crushers, locking device for intestinal clamp, needle holder, gastro-urology hook, gastro-urology probe and director, nonself-retaining retractor, laparotomy rings, nonelectrical snare, rectal specula, bladder neck spreader, self-retaining retractor, and scoop.
• Gastroenterologic Needle Holder (FDA Code: FHQ / 876.4730)
• General & Plastic Saw Surgical Blade (FDA Code: GFA / 878.4820)
• General & Plastic Surgery Forceps (FDA Code: GEN / 878.4800)
• General & Plastic Surgery Mirror (FDA Code: FTX / 878.4800)
• General & Plastic Surgery Surgical Burr (FDA Code: GFF / 878.4820)
• General & Plastic Surgery Surgical Cannula (FDA Code: GEA / 878.4800)
• General & Plastic Surgery Surgical Clamp (FDA Code: GDJ / 878.4800)
• General & Plastic Surgery Surgical Dissector (FDA Code: GDI / 878.4800)
• General & Plastic Surgery Surgical Elevator (FDA Code: GEG / 878.4800)
• General & Plastic Surgery Surgical File (FDA Code: GEO / 878.4800)
• General & Plastic Surgery Surgical Gouge (FDA Code: GDH / 878.4800)
• General & Plastic Surgery Surgical Hook (FDA Code: GDG / 878.4800)
• General & Plastic Surgery Surgical Mallet (FDA Code: GFJ / 878.4800)
• General & Plastic Surgery Surgical Rasp (FDA Code: GAC / 878.4800)
• General & Plastic Surgery Surgical Spatula (FDA Code: GAF / 878.4800)
• General Surgical Manual Instrument (FDA Code: MDM / 878.4800)
• General use Surgical Curettes (FDA Code: FZS / 878.4800)
• Gynecological Biopsy Forceps (FDA Code: HFB / 884.4530)
• Inflation Bulb For Endoscope (FDA Code: FCY / 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.
• Manual Cast Application and Removal Instrument (FDA Code: LGG / 888.5980)
A manual cast application and removal instrument is a nonpowered hand-held device intended to be used in applying or removing a cast. This generic type of device includes the cast knife, cast spreader, plaster saw, plaster dispenser, and casting stand.
• Manual Gastro-Urology Surgical Instrument (FDA Code: KOA / 876.4730)
• Manual Saw & Accessories (FDA Code: GDR / 878.4800)
• Metal Vaginal Speculum (FDA Code: HDF / 884.4520)
• Metal/Plastic Urethral Sound (FDA Code: FBX / 876.5520)
A urethral dilator is a device that consists of a slender hollow or solid instrument made of metal, plastic, or other suitable material in a cylindrical form and in a range of sizes and flexibilities. The device may include a mechanism to expand the portion of the device in the urethra and indicate the degree of expansion on a dial. It is used to dilate the urethra. This generic type of device includes the mechanical urethral dilator, urological bougies, metal or plastic urethral sound, urethrometer, filiform, and filiform follower.
• Mouth Gags (FDA Code: KBN / 874.4420)
• Nasal Knife (FDA Code: KAS / 874.4420)
• Nasal Rasps (FDA Code: KBA / 874.4420)
• Nasal Rongeur (FDA Code: KBB / 874.4420)
• Nasal Saw (FDA Code: KBC / 874.4420)
• Nasal Scissors (FDA Code: KBD / 874.4420)
• Nasal Scissors Straight (FDA Code: KBD / 874.4420)
• Nasal Snare (FDA Code: KBE / 874.4420)
• Non-Electric Biopsy Forceps (FDA Code: FCL / 876.1075)
A gastroenterology-urology biopsy instrument is a device used to remove, by cutting or aspiration, a specimen of tissue for microscopic examination. This generic type of device includes the biopsy punch, gastrointestinal mechanical biopsy instrument, suction biopsy instrument, gastro-urology biopsy needle and needle set, and nonelectric biopsy forceps. This section does not apply to biopsy instruments that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.

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