NKK

Product Code: NKK

Products Classified as NKK

2694

Needle, Hypodermic, Single Lumen, Reprocessed

Hypodermic Single Lumen Needle.

Total Product Life Cycle (TPLC) Devices

2694

Needle, Hypodermic, Single Lumen, Reprocessed

Hypodermic Single Lumen Needle.

FDA Consensus Standards

• Needle, Hypodermic, Single Lumen, Reprocessed [31768]: 21 CFR §880.5570 🔎

Global Unique Device Identification Database

• 00380658175016: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
• 00380658172015: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
• 00380658170011: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
• 00380657517954: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
• 10380657409706: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
• 10380657409690: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
• 00380657510139: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
• 00380657510122: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
• 00850033297010: Needle, Hypodermic, Single Lumen, Reprocessed
• G079C5020000450: Needle, Hypodermic, Single Lumen, Reprocessed

Maude Adverse Events

MONOJECT LIFESHIELD	COVIDIEN LLC	2019-10-25
SAFETY NEEDLE	COVIDIEN	2017-06-25
DRAGONFLY IMAGING CATHETER	ST. JUDE MEDICAL	2012-09-19
DRAGONFLY IMAGING CATHETER	ST. JUDE MEDICAL	2012-08-07
DRAGONFLY IMAGING CATHETER	ST. JUDE MEDICAL	2012-06-25
QUIXIL APPLICATION DEVICE	OMRIX BIOPHARMACEUTICALS LTD.	2009-12-03