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Address: 931 Progress Ave. Ste.13, Scarborough, Ontario M1G 3V5, Canada
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Phone: +1-(416)-439-2237, 800-565-4336
Year Established: 1994
Annual Revenues: < USD 1 Million
Employee Count: ~10
Quality: CE Certified
Products: Abdominal Binders (FDA Code:
FSD), Bariatric Abdominal Binder, Panel Elastic Abdominal Binder, Femoral Leg Traction Splint, Non-Inflatable Compression Legging (FDA Code:
LLK), Handicapped/Disabled Reacher, ...
Geen Healthcare Inc. offers skin cleaner and conditioner, pressure free socks for diabetic patients, medical containers, instrument holders, and speed splint.
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Address: Rua Da Paz, 1629-Bairro, N.S. Aparecida, Flores Da Cunha CEP 95270, Brazil
Phone: +54-(292)-1024
Products: Traction Splint (FDA Code:
HSP), Hand-Carried Stretcher (FDA Code:
FPP), Manual Patient Transfer Device (FDA Code:
FMR), Wheeled (Mobile) Stretcher (FDA Code:
FPO), ...
Sitmed Equipamento Medicos Ltda. specializes in offering manual patient transfer devices, wheeled stretchers and traction splints.
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Address: 495 Blackburn Rd., Mount Waverley, Melbourne, Victoria, Australia
Phone: +61-(3)-921-1 74
FDA Registration: 8020030
Products: Analyte Specific Reagents, Asr Reagents (FDA Code:
MVU), Automated Slide Stainer (FDA Code:
KPA), Automated Tissue Processor (FDA Code:
IEO), Femoral Leg Traction Splint, Estrogen Receptor Antibody Immunohistochemistry Assay (FDA Code:
MYA), General Purpose Reagent (FDA Code:
LDT), ...
Vision Instruments Ltd. offers tissue processors. Our products include analytic specific reagents, automated slide stainer, automated tissue processor, and general purpose reagents. We also provide ha
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FDA Code / Regulation: HSP / 888.5890 A noninvasive traction component is a device, such as a head halter, pelvic belt, or a traction splint, that does not penetrate the skin and is intended to assist in connecting a patient to a traction apparatus so that a therapeutic pulling force may be applied to the patient's body.
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 888.9. The device is also 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, regarding general requirements concerning records, and 820.198, regarding complaint files.