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 Bronchial Suction Latex Rubber Catheter Suppliers > General Surgical Co., (india) Pvt. Ltd.

General Surgical Co., (india) Pvt. Ltd.

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Web: http://www.gescoindia.com
E-Mail:
Address: G-6 Gee Cee Crescent, 114, Ponamallee High Road, Chennai, Tamil Nadu 60084, India
Phone: +91-(44)-2825 96 02 | Fax: +91-(44)-2825 94 39 | Map/Directions >>
 
 

Profile: General Surgical Co., (india) Pvt. Ltd. is a manufacturer of surgical instruments. We produce medical & surgical disposables, general, ENT, neuro & spinal, orthopedic, gynecology & obstetrics, plastic, cardio thoracic, urology, oncology, vascular, ophthalmic, dental, oral & maxillofacial surgery instruments.

The company is ISO 9001:2000 certified.

FDA Registration Number: 9613926
US Agent: David Lennarz / Registrar Corp
Phone: +1-(757)-224-0177  Fax: +1-(757)-224-0179  E-Mail:

101 to 150 of 560 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 2 [3] 4 5 6 7 8 9 10 11 12 >> Next 50 Results
• Ear Suction Tube (FDA Code: JZF / 874.4420)
• 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.
• Ear-Lobe Perforator (FDA Code: JYS / 874.4420)
• Electric Cystometric Table (FDA Code: MMZ / 876.4890)
A urological table and accessories is a device that consists of a table, stirrups, and belts used to support a patient in a suitable position for endoscopic procedures of the lower urinary tract. The table can be adjusted into position manually or electrically.
• Electrically-Powered Surgical Sponge Scale (FDA Code: MRL / 880.2740)
A surgical sponge scale is a nonelectrically powered device used to weigh surgical sponges that have been used to absorb blood during surgery so that, by comparison with the known dry weight of the sponges, an estimate may be made of the blood lost by the patient during surgery.
• Electrode Cables (FDA Code: IKD / 890.1175)
An electrode cable is a device composed of strands of insulated electrical conductors laid together around a central core and intended for medical purposes to connect an electrode from a patient to a diagnostic machine.
• Eletric/Pneumatic ENT Surgical Saw (FDA Code: EWQ / 874.4420)
• 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.
• Endoscopic Non-Prescription Lens Eyepiece (FDA Code: FEI / 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.
• Endoscopic Teaching Attachment (FDA Code: FEA / 876.1500)
• ENT Applicator (FDA Code: KCJ / 874.5220)
• ENT Dropper (FDA Code: KCM / 874.5220)
• ENT Drug Applicator (FDA Code: LRD / 874.5220)
• ENT Elevator (FDA Code: KAD / 874.4420)
• ENT Esophageal Bougie (FDA Code: KCD / 874.4420)
• ENT Esophageal Dilator (FDA Code: KCF / 874.4420)
• ENT Examining/Treatment Unit (FDA Code: ETF / 874.5300)
An ear, nose, and throat examination and treatment unit is an AC-powered device intended to support a patient during an otologic examination while providing specialized features for examination and treatment. The unit consists of a patient chair and table, drawers for equipment, suction and blowing apparatus, and receptacles for connection of specialized lights and examining instruments.
• ENT Forceps (FDA Code: KAE / 874.4420)
• ENT Irrigation Syringe (FDA Code: KCP / 874.5220)
• ENT Knife (FDA Code: KTG / 874.4420)
• ENT Manual Surgical Instrument (FDA Code: LRC / 874.4420)
• Ent Microrule (FDA Code: KAH / 874.4420)
• ENT Mirror (FDA Code: KAI / 874.4420)
• ENT Mobilizer (FDA Code: KAJ / 874.4420)
• ENT Nasal Gouge (FDA Code: KAQ / 874.4420)
• ENT Powder Blower (FDA Code: KCL / 874.5220)
• ENT Probe (FDA Code: KAK / 874.4420)
• ENT Punch (FDA Code: KTF / 874.4420)
• ENT Retractor (FDA Code: KAL / 874.4420)
• ENT Speculum Holder (FDA Code: KAG / 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.
• ENT Surgical Tray (FDA Code: MMO / 874.4420)
• ENT Syringe (FDA Code: KCP / 874.5220)
• ENT Tracheal Hook (FDA Code: KCH / 874.4420)
• ENT Trocar (FDA Code: KTE / 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:
• 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.
• Erisophake (FDA Code: HNT / 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.
• Ethmoid Curettes (FDA Code: KAO / 874.4420)
• Ethmoid Punch (FDA Code: KAX / 874.4420)
• Eustachian Bougie (FDA Code: KBI / 874.4175)
A nasopharyngeal catheter is a device consisting of a bougie or filiform catheter that is intended for use in probing or dilating the eustachian tube. This generic type of device includes eustachian catheters.
• Eustachian Filliform Set (FDA Code: KBY / 874.4175)
• Examination and Treatment Chair (FDA Code: FRK / 880.6140)
A medical chair or table is a device intended for medical purposes that consists of a chair or table without wheels and not electrically powered which, by reason of special shape or attachments, such as food trays or headrests, or special features such as a built-in raising and lowering mechanism or removable arms, is intended for use of blood donors, geriatric patients, or patients undergoing treatment or examination.
• Expressor (FDA Code: HNS / 886.4350)
• External Aesthetic Restoration Material (FDA Code: GBI / 878.3800)
An external aesthetic restoration prosthesis is a device intended to be used to construct an external artificial body structure, such as an ear, breast, or nose. Usually the device is made of silicone rubber and it may be fastened to the body with an external prosthesis adhesive. The device is not intended to be implanted.
• External Ankle Brace (FDA Code: ITW / 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.
• External Brace Component Stirrup (FDA Code: ITC / 890.3410)
An external limb orthotic component is a device intended for medical purposes for use in conjunction with an orthosis (brace) to increase the function of the orthosis for a patient's particular needs. Examples of external limb orthotic components include the following: A brace-setting twister and an external brace stirrup.
• External Brace Hip Joint (FDA Code: ITS / 890.3475)
• External Brace Knee Joint (FDA Code: ITQ / 890.3475)
• External Breast Prosthesis (FDA Code: KCZ / 878.3800)
• External Component Thigh Socket Prosthesis (FDA Code: ISS / 890.3420)
An external limb prosthetic component is a device intended for medical purposes that, when put together with other appropriate components, constitutes a total prosthesis. Examples of external limb prosthetic components include the following: Ankle, foot, hip, knee, and socket components; mechanical or powered hand, hook, wrist unit, elbow joint, and shoulder joint components; and cable and prosthesis suction valves.

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