Exmoor Plastics Limited

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Contact: Margaret Blackmore
Web: http://www.exmoorplastics.co.uk
E-Mail:
Address: Lisieux Way, Taunton TA1 2LB, United Kingdom
Phone: +44-(1823)-351040 | Fax: +44-(1823)-334154 | Map/Directions >>

Profile: Exmoor Plastics Limited designs, develops, and manufactures sterile surgical & microsurgical devices. We provide procedure packs, diathermy devices, ear prostheses and ear bone harvester products. Our procedure packs are single-use myringotomy kits which combines the unique Exmoor suction equipment with Exmoor aural ventilation tubes and a wide selection of other components. We offer suction clearance kits, tympanocentesis kits and tonsillectomy kits. Our diathermy devices are bipolar forceps and mono polar suction devices. We develop BK/40/PL straight and BK/41/PL bayonet which features with rigid blades 200mm/8inch, fine tips, 3m integral cables, meet electrical standard, suited to electro-surgical generators, standard pack of 10 devices and avoids the risk of iatrogenic cross-infection of prion disease-especially important in tonsillectomy procedures.

FDA Registration Number: 3002806953
US Agent: Patty Crull
Phone: +1-(317)-243-7171 E-Mail:

15 Products/Services (Click for related suppliers)

• Bone Particle Collector (FDA Code: MXP / 874.4800)

A bone particle collector is a filtering device intended to be inserted into a suction tube during the early stages of otologic surgery to collect bone particles for future use.

• Dental Protector (FDA Code: BRW / 868.5820)

A dental protector is a device intended to protect a patient's teeth during manipulative procedures within a patient's oral cavity.

• 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 Suction Tube (FDA Code: JZF / 874.4420)

• ENT Irrigation Syringe (FDA Code: KCP / 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.

• ENT Manual Surgical Instrument (FDA Code: LRC / 874.4420)

• ENT Synthetic Polyamide Polymer (FDA Code: KHJ / 874.3620)

Ear, nose, and throat synthetic polymer material is a device material that is intended to be implanted for use as a space-occupying substance in the reconstructive surgery of the head and neck. The device is used, for example, in augmentation rhinoplasty and in tissue defect closures in the esophagus. The device is shaped and formed by the suregon to conform to the patient's needs. This generic type of device is made of material such as polyamide mesh or foil and porous polyethylene.

• ENT Syringe (FDA Code: KCP / 874.5220)

• 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.

• Myringotomy Tube Inserter (FDA Code: JYM / 874.4420)

• Non-Sterile Absorbent Tipped Applicator (FDA Code: KXF / 880.6025)

An absorbent tipped applicator is a device intended for medical purposes that consists of an absorbent swab on a wooden, paper, or plastic stick. The device is used to apply medications to, or to take specimens from, a patient.

• Powered Surgical Laser Instrument (FDA Code: GEX / 878.4810)

(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.

• Soft Ear Speculum (FDA Code: EPY / 878.1800)

• Tonsillectome (FDA Code: KCA / 874.4420)

• 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.