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Gimmi GmbH

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Web: http://www.gimmi.de
E-Mail:
Address: Carl-Zeiss-Strasse 6, Tuttlingen, Baden-Wuerttemberg D-78532, Germany
Phone: +49-(7461)-96 590-0 | Fax: +49-(7461)-96 590-33 | Map/Directions >>
 
 

Profile: Gimmi GmbH manufactures and distributes medical products. We specialize in instruments & equipment for endoscopy. Our product line ranges from instruments for general surgery to our developed endoscopic equipment and accessories.

The company has revenues of < USD 1 Million, has ~20 employees and is ISO 9001, CE certified.

FDA Registration Number: 3010607620
US Agent: Kenneth Blake / Scanlan International Inc.
Phone: +1-(651)-298-0997  E-Mail:

201 to 243 of 243 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 2 3 4 [5]
• Semi Rigid biopsy forceps
• Sinuscopes
• Skin Marker (FDA Code: FZZ / 878.4660)
A skin marker is a pen-like device intended to be used to write on the patient's skin, e.g., to outline surgical incision sites or mark anatomical sites for accurate blood pressure measurement.
• Skull Punch (FDA Code: GXJ / 882.4750)
A skull punch is a device used to punch holes through a patient's skull to allow fixation of cranioplasty plates or bone flaps by wire or other means.
• Soft 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.
• Standard Oval Biopsy Forceps
• Sterile Container System
• Suction Catheter and Tip (FDA Code: JOL / 880.6740)
A vacuum-powered body fluid suction apparatus is a device used to aspirate, remove, or sample body fluids. The device is powered by an external source of vacuum. This generic type of device includes vacuum regulators, vacuum collection bottles, suction catheters and tips, connecting flexible aspirating tubes, rigid suction tips, specimen traps, noninvasive tubing, and suction regulators (with gauge).
• Surgical Curette (FDA Code: FZS / 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.
• Surgical Instrument (Miscellaneous Medical)
• Surgical Instrument Tray (FDA Code: FSM / 878.4800)
• Surgical Knife (FDA Code: EMF / 878.4800)
• Surgical Needle Guide (FDA Code: GDF / 878.4800)
• Surgical Ophthalmic 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.
• Surgical Orthopedic Scissors (FDA Code: HRR / 888.4540)
An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.
• Surgical Retractor (FDA Code: GAD / 878.4800)
• Surgical Retractor Systems (FDA Code: GAD / 878.4800)
• Surgical Skin Markers (FDA Code: FZZ / 878.4660)
• Surgical Stripper (FDA Code: HRT / 888.4540)
• Tamps (FDA Code: HXG / 888.4540)
• Thoracoscopes
• Titanium Microsurgical Instruments
• Tongue Depressors (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.
• Tonsil Knife (FDA Code: KBQ / 874.4420)
• Tonsil Punch (FDA Code: KBT / 874.4420)
• Tonsil Snares (FDA Code: KBZ / 874.4420)
• Tracheal Dilators (FDA Code: KCG / 874.4420)
• Tracheal Tube Cleaning Brushes (FDA Code: EPE / 868.5795)
A tracheal tube cleaning brush is a device consisting of a brush with plastic bristles intended to clean tracheal cannula devices after their removal from patients.
• Tuning Forks (FDA Code: GWX / 882.1525)
A tuning fork is a mechanical device which resonates at a given frequency and is used to diagnose hearing disorders and to test for vibratory sense.
• Umbilical Scissors (FDA Code: HDJ / 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:
• Ureteroscopic Biopsy Forceps
• Urethral Dilators (FDA Code: KOE / 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.
• Urethroscope (FDA Code: FGC / 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.
• Urethrotome (FDA Code: EZO / 876.4770)
A urethrotome is a device that is inserted into the urethra and used to cut urethral strictures and enlarge the urethra. It is a metal instrument equipped with a dorsal-fin cutting blade which can be elevated from its sheath. Some urethrotomes incorporate an optical channel for visual control.
• Urological Bougie (FDA Code: FAX / 876.5520)
• Urological Catheters (FDA Code: KOD / 876.5130)
A urological catheter and accessories is a flexible tubular device that is inserted through the urethra and used to pass fluids to or from the urinary tract. This generic type of device includes radiopaque urological catheters, ureteral catheters, urethral catheters, coudecatheters, balloon retention type catheters, straight catheters, upper urinary tract catheters, double lumen female urethrographic catheters, disposable ureteral catheters, male urethrographic catheters, and urological catheter accessories including ureteral catheter stylets, ureteral catheter adapters, ureteral catheter holders, ureteral catheter stylets, ureteral catheterization trays, and the gastro-urological irrigation tray (for urological use).
• Uterine Biopsy Forceps
• Uterine Curettes (FDA Code: HCY / 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:
• Wire Cutters (FDA Code: HXZ / 888.4540)
• Wire Holding Forceps (FDA Code: HYA / 878.4800)
• Wire Twisters (FDA Code: HXS / 888.4540)
• Xenon Arc Endoscope Light Source (FDA Code: GCT / 876.1500)
• Yasargil Aneurysm Clips

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