FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS. The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies.
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Dental Piezo Bone Surgery Machine. Piezo Surgery Dental Motor. FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS. Power Source.
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Dental Piezo Bone Surgery Machine. Place of Origin. Shelf Life. Piezo Surgery Dental Motor. Safety standard. Model Number. The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies.
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Dental Piezo Bone Surgery Machine. Place of Origin. Shelf Life. Piezo Surgery Dental Motor. Safety standard. Model Number. The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies.
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GreatLife Dent Dental Surgic Touch Ultrasonic Bone Surgery Unit Piezo Bone Cutter Implant Motor Ultrasurgery Piezosurgery Device.
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GreatLife Dent Dental Implant Surgical Motor Surgic LED Touch Screen Implant Motor 20:1 Handpiece Bone Surgery Electric System.
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The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. City,State:BEIJING,China.
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The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. City,State:BEIJING,China.
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