EXEL Spinal Needle 26961

GUDID 20020221269615

Spinal Needle, 20G x 2-3/4, QUINCKE BEVEL

Exel International

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• Primary Device ID: 20020221269615
• NIH Device Record Key: f4bb8ebc-d6c4-4f7a-bb03-8cdb0583fdb3
• Commercial Distribution Discontinuation: 2023-04-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: EXEL Spinal Needle
• Version Model Number: 26961
• Catalog Number: 26961
• Company DUNS: 180572216
• Company Name: Exel International
• Device Count: 50
• 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	00020221269611 [Unit of Use]
GS1	10020221269618 [Primary]
GS1	20020221269615 [Package]; Contains: 10020221269618; Package: [2 Units]; Discontinued: 2023-04-21; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K895771

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: 3
• Public Version Date: 2023-04-24
• Device Publish Date: 2016-09-23

On-Brand Devices [EXEL Spinal Needle]

• 20020221269653: Spinal Needle, 22G x 2 3/4, QUINCKE BEVEL
• 20020221269707: Spinal Needle, 25G x 3 1/2, QUINCKE BEVEL
• 20020221269677: Spinal Needle, 22G x 3 1/2, QUINCKE BEVEL
• 20020221269646: Spinal Needle, 20G x 3 1/2, QUINCKE BEVEL
• 10020221269601: Spinal Needle, 18G x 3 1/2, QUINCKE BEVEL
• 20020221269615: Spinal Needle, 20G x 2-3/4, QUINCKE BEVEL