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Address: 42 Xixin Rd., Zhangjing Town, Wuxi City, China
Phone: +86-(510)-83791681
Products: Tongue Depressors (FDA Code:
FMA), Blood pressure Cuffs (FDA Code:
DXQ), Clinical Mercury Thermometers (FDA Code:
FLK), Sweetened Tongue Depressors, Used Tongue Depressors, Neonatal Disposable Blood Pressure Cuffs, ...
Golden Horse Medical Equipment (Wuxi) Co. Ltd. manufactures OEM diagnostic medical products and accessories. Our product range includes stethoscopes, sphygmomanometers, clinical thermometers, neurolog
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Address: 4056 North Service Road, Windsor, Ontario N8W 5X2, Canada
www.boviemed.com |
Phone: +1-(519)-251-0668
Products: Forceps (FDA Code:
HTD), Arthroscopes (FDA Code:
HRX), Drill Bit (FDA Code:
HTW), Tracheal Tube Stylet (FDA Code:
BSR), Electrosurgical Cutting and Coagulation Device (FDA Code:
GEI), Electrosurgical Electrode (FDA Code:
JOS), ...
Bovie Medical Corporation specializes in offering surgi-center and hospital-based electrosurgical generators & accessories. We offer a full line of disposable electrosurgical electrodes in blade, ball
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Address: 35 Stirling St., Thebarton, Adelaide, SA 5031, Australia
www.scanoptics.com.au |
Send Inquiry |
Phone: +61-(8)-8234-9120
FDA Registration: 3002562003
Products: Battery-Powered Medical Examination Light (FDA Code:
KYT), AC-Powered Biomicroscope Slit Lamp (FDA Code:
HJO), AC-Powered Ophthalmoscope (FDA Code:
HLI), Ophthalmic AC-Powered Operating Microscope and Accessories (FDA Code:
HRM), Ophthalmic Operating Spectacle (FDA Code:
HOH), ...
Scan Optics Pty., Ltd. is associated with microscopes, surgical lights, slit lamps, ophthalmoscopes and accessories. Our SO-111T ophthalmic microscope is a small microscope for use in the operating ro
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63 Battery-Powered Medical Examination Light suppliers Page:
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FDA Code / Regulation: KYT / 880.6350 A battery-powered medical examination light is a battery-powered device intended for medical purposes that is used to illuminate body surfaces and cavities during a medical examination.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 880.9. The device also is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, with respect to general requirements concerning records, and 820.198, with respect to complaint files.