Curity 1048

GUDID 20884521020365

Pediatric Lumbar Puncture Tray with Safety Components

Cardinal Health, Inc.

Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit Lumbar puncture kit

• Primary Device ID: 20884521020365
• NIH Device Record Key: 5c6c76df-8adc-4476-b461-aad81fe70d47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curity
• Version Model Number: 1048
• Catalog Number: 1048
• Company DUNS: 080935429
• Company Name: Cardinal Health, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521020368 [Primary]
GS1	20884521020365 [Package]; Contains: 10884521020368; Package: CASE [10 Units]; In Commercial Distribution

FDA Product Code

• FMJ: MANOMETER, SPINAL-FLUID

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2023-03-23
• Device Publish Date: 2016-09-24

On-Brand Devices [Curity]

• 00884521060541: All Purpose Sponges,Non-woven, 4 Ply
• 00884521060510: All Purpose Sponges,Non-woven, 4 Ply
• 10884521060388: All Purpose Sponges,Nonwoven, 4 Ply
• 10884521000186: AMD Antimicrobial Packing Strips,0.2% Polyhexamethylene Biguanide HCI (PHMB)
• 20884521006604: AMD Antimicrobial Packing Strips,0.2% Polyhexamethylene Biguanide HCI (PHMB)
• 20884521006598: AMD Antimicrobial Packing Strips,0.2% Polyhexamethylene Biguanide HCI (PHMB)
• 30884527020625: Alcohol Prep,2 Ply, Medium
• 20884521134024: Gauze Sponges,16 Ply
• 20884521099675: Gauze Sponges,12 Ply
• 20884521083940: Gauze Pad
• 20884521068695: Plain Packing Strip
• 20884521068688: Plain Packing Strip
• 20884521068671: Plain Packing Strip
• 20884521068664: Plain Packing Strip
• 20884521060309: All Purpose Sponges,Nonwoven, 4 Ply
• 10884521060289: Gauze Pad
• 10884521060265: Gauze Pads
• 20884521059358: Dressing Sponges,6 Ply
• 20884527016348: Bandage Roll
• 10884527008445: X-Ray Detectable Laparotomy Sponges,Tray Pack
• 10884527001125: 100% Cotton OB Sponges,Moderate
• 10884527001118: 100% Cotton OB Sponges,Moderate
• 10884527001101: 100% Cotton OB Sponges,Moderate
• 10884527001064: Cleaners,Large,Moderate
• 10884521157675: Winged Peri-Pad,Moderate
• 10884521157668: Peri-Pad,Moderate
• 10884521144736: Adhesive Bandage
• 10884521144460: Flexible Adhesive Bandage
• 10884521109469: Hypoallergenic Clear Tape
• 10884521109407: Hypoallergenic Clear Tape
• 10884521104723: Hypoallergenic Clear Tape
• 10884521064874: Multi Trauma Dressing
• 30884521060290: Gauze Pad
• 50192253002063: True content to be populated as part of rebranding
• 20884521068732: Iodoform Packing Strip
• 20884521068725: Iodoform Packing Strip
• 20884521068718: Iodoform Packing Strip
• 20884521068701: Iodoform Packing Strip
• 20884527020581: Eye Pad,Oval
• 20884521109275: Hypoallergenic Clear Tape
• 20884527016669: Sodium Chloride Dressing
• 50885380174900: True content to be populated as part of rebranding
• 50885380174894: True content to be populated as part of rebranding
• 50885380174887: True content to be populated as part of rebranding
• 30885380174692: True content to be populated as part of rebranding
• 30885380174685: True content to be populated as part of rebranding
• 30885380174678: True content to be populated as part of rebranding
• 50885380174665: True content to be populated as part of rebranding
• 30885380174654: True content to be populated as part of rebranding
• 30885380174647: True content to be populated as part of rebranding