Nipro SafeTouch TULIP Safety Fistula Needle

GUDID 10383790000397

SafeTouch Tulip Safety AVF (15Gx1-1/4") 12" tube, rotating hub

NIPRO MEDICAL CORPORATION

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• Primary Device ID: 10383790000397
• NIH Device Record Key: 62acfcc6-1b0b-4307-a044-5c09bffa6775
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nipro SafeTouch TULIP Safety Fistula Needle
• Version Model Number: FT+153230BCR
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com
• Phone: (908) 393-7030
• Email: info@nipromed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00383790000390 [Primary]
GS1	10383790000397 [Package]; Contains: 00383790000390; Package: box [50 Units]; In Commercial Distribution
GS1	40383790000398 [Package]; Package: case [6 Units]; In Commercial Distribution

FDA Product Code

• MPB: Catheter, Hemodialysis, Non-Implanted

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: 2023-09-25
• Device Publish Date: 2023-09-15

On-Brand Devices [Nipro SafeTouch TULIP Safety Fistula Needle]

• 10383790001790: SafeTouch Tulip Safety AVF (16Gx1") 16" tube, fixed hub
• 10383790001776: SafeTouch Tulip Safety AVF (15Gx1") 16" tube, fixed hub
• 00383790000581: SafeTouch Tulip Safety AVF (17Gx1-1/4") 12" tube, fixed hub (twin pack)
• 00383790000567: SafeTouch Tulip Safety AVF (16Gx1-1/4") 12" tube, fixed hub (twin pack)
• 00383790000543: SafeTouch Tulip Safety AVF (15Gx1-1/4") 12" tube, fixed hub (twin pack)
• 00383790000529: SafeTouch Tulip Safety AVF (17Gx1") 12" tube, fixed hub (twin pack)
• 10383790000496: SafeTouch Tulip Safety AVF (17Gx1") 12" tube, rotating hub
• 10383790000489: SafeTouch Tulip Safety AVF (17Gx1") 12" tube, fixed hub
• 00383790000468: SafeTouch Tulip Safety AVF (16Gx1") 12" tube, fixed hub (twin pack)
• 10383790000441: SafeTouch Tulip Safety AVF (16Gx1-1/4") 12" tube, fixed hub
• 10383790000434: SafeTouch Tulip Safety AVF (16Gx1") 12" tube, rotating hub
• 10383790000427: SafeTouch Tulip Safety AVF (16Gx1") 12" tube, fixed hub
• 00383790000406: SafeTouch Tulip Safety AVF (15Gx1") 12" tube, fixed hub (twin pack)
• 10383790000397: SafeTouch Tulip Safety AVF (15Gx1-1/4") 12" tube, rotating hub
• 10383790000380: SafeTouch Tulip Safety AVF (15Gx1-1/4") 12" tube, fixed hub
• 10383790000373: SafeTouch Tulip Safety AVF (15Gx1") 12" tube, rotating hub
• 10383790000366: SafeTouch Tulip Safety AVF (15Gx1") 12" tube, fixed hub
• 00383790000345: SafeTouch Tulip Safety AVF (14Gx1") 12" tube, fixed hub (twin pack)
• 10383790000304: SafeTouch Tulip Safety AVF (14Gx1") 12" tube, fixed hub