Nipro SafeTouch IV Catheter

GUDID 10383790011300

Safety IV Catheter, Straight type (24Gx3/4")

NIPRO MEDICAL CORPORATION

Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula

• Primary Device ID: 10383790011300
• NIH Device Record Key: ef8d2cb4-8afe-410e-8b0f-d2fc884ff109
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nipro SafeTouch IV Catheter
• Version Model Number: NI-CSF2419PET
• Company DUNS: 797372554
• Company Name: NIPRO MEDICAL CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com
• Phone: +1 908-393-7030
• Email: info@nipromed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00383790011303 [Primary]
GS1	10383790011300 [Package]; Contains: 00383790011303; Package: Box [50 Units]; In Commercial Distribution
GS1	40383790011301 [Package]; Package: Case [40 Units]; In Commercial Distribution

FDA Product Code

• FOZ: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-24
• Device Publish Date: 2022-10-15

On-Brand Devices [Nipro SafeTouch IV Catheter]

• 40383790009698: 24G x 1”, Winged, 21 ml/min
• 40383790009681: 24G x 3/4”, Winged, 21 ml/min
• 40383790009674: 22G x 1 1/4”, Winged, 36 ml/min
• 40383790009667: 22G x 1”, Winged, 36 ml/min
• 40383790009650: 20G x 2”, Winged, 54 ml/min
• 40383790009643: 20G x 1 1/4”, Winged, 54 ml/min
• 40383790009636: 18G x 2”, Winged, 90 ml/min
• 40383790009629: 18G x 1 1/4”, Winged, 90 ml/min
• 40383790009612: 16G x 2”, Winged, 180 ml/min
• 10383790011300: Safety IV Catheter, Straight type (24Gx3/4")
• 10383790011157: Safety IV Catheter, Straight type (24Gx1")
• 10383790011140: Safety IV Catheter, Straight type (22Gx1 1/4")
• 10383790011133: Safety IV Catheter, Straight type (22Gx1")
• 10383790011126: Safety IV Catheter, Straight type (20Gx2")
• 10383790011119: Safety IV Catheter, Straight type (20Gx1 1/4")
• 10383790011102: Safety IV Catheter, Straight type (18Gx2")
• 10383790011096: Safety IV Catheter, Straight type (18Gx1 1/4")
• 10383790011089: Safety IV Catheter, Straight type (16Gx2")