Kurin Blood Collection Set, 23 Ga, Push Button Needle, BioMerieux

GUDID 20851682007061

PATHWAY, LLC

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• Primary Device ID: 20851682007061
• NIH Device Record Key: 74f137fb-166e-4495-ab8b-5991a9fbbebe
• Commercial Distribution Discontinuation: 2018-07-23
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Kurin Blood Collection Set, 23 Ga, Push Button Needle, BioMerieux
• Version Model Number: M-21223
• Company DUNS: 080312381
• Company Name: PATHWAY, LLC
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851682007067 [Primary]
GS1	10851682007064 [Package]; Contains: 00851682007067; Package: [50 Units]; Discontinued: 2018-07-23; Not in Commercial Distribution
GS1	20851682007061 [Package]; Contains: 10851682007064; Package: [4 Units]; Discontinued: 2018-07-23; Not in Commercial Distribution

FDA Product Code

• JKA: Tubes, Vials, Systems, Serum Separators, Blood Collection

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-23
• Device Publish Date: 2017-03-13

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