NIPRO SafeTouch™ Safety Scalp Vein Set

GUDID 10383790002599

NIPRO MEDICAL CORPORATION

Scalp vein needle

• Primary Device ID: 10383790002599
• NIH Device Record Key: 0014d9f2-d7f3-4748-a6fe-72c436cb1964
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NIPRO SafeTouch™ Safety Scalp Vein Set
• Version Model Number: SPR+21G19
• 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: +1 (908) 393-7030
• Email: info@nipromed.com
• Phone: +1 (908) 393-7030
• Email: info@nipromed.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00383790002592 [Primary]
GS1	10383790002599 [Package]; Contains: 00383790002592; Package: [50 Units]; In Commercial Distribution
GS1	40383790002590 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• FMI: Needle, hypodermic, single lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-16

On-Brand Devices [NIPRO SafeTouch™ Safety Scalp Vein Set]

• 40383790002613: SPR+25G19
• 10383790002605: SPR+23G19
• 10383790002599: SPR+21G19
• 40383790002583: SPR+19G19