NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED

FDA product code NKK · Class 2 · 6 devices · 47 reports · 0 devices named in recalls

• ULTRA FLOW 8065751795

  Alcon Laboratories, Inc. · NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
  22 reports
• INTREPID® 8065751013

  Alcon Laboratories, Inc. · NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
  10 reports
• INTREPID® 8065751012

  Alcon Laboratories, Inc. · NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
  8 reports
• ALCON 8065740970

  Alcon Laboratories, Inc. · NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
  3 reports
• ALCON 8065740969

  Alcon Laboratories, Inc. · NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
  2 reports
• ULTRA FLOW 00380658170011

  Alcon Laboratories, Inc. · NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
  2 reports