SteriPath Gen2, 23G 2700-23-EN

GUDID 10858366007020

SteriPath Gen2 Blood Collection System, Sterile Pack, 23G

Magnolia Medical Technologies, Inc.

Blood transfer set

• Primary Device ID: 10858366007020
• NIH Device Record Key: 02134884-ff15-44d4-990b-038a3bf1106d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SteriPath Gen2, 23G
• Version Model Number: 2700-23-EN
• Catalog Number: 2700-23-EN
• Company DUNS: 078603710
• Company Name: Magnolia Medical Technologies, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: true
• 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	00858366007023 [Primary]
GS1	10858366007020 [Package]; Contains: 00858366007023; Package: Sales Pack [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192247

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: 2
• Public Version Date: 2021-04-07
• Device Publish Date: 2020-11-06

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