Spine Needle and Cannula

GUDID 05060696460071

DC 19 ga x 3” Cannula (10)

MORGAN STEER ORTHOPAEDICS LIMITED

Needle guide, single-use

• Primary Device ID: 05060696460071
• NIH Device Record Key: c30d5c42-159f-49b7-accb-b5bdd57d9586
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spine Needle and Cannula
• Version Model Number: KNS-1904-10
• Company DUNS: 216776681
• Company Name: MORGAN STEER ORTHOPAEDICS LIMITED
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060696460071 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061259

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2024-06-11
• Device Publish Date: 2024-06-03

On-Brand Devices [Spine Needle and Cannula]

• 05060696460095: Crawford 17 ga x 8” cannula (1)
• 05060696460088: Crawford 17 ga x 6” cannula (1)
• 05060696460071: DC 19 ga x 3” Cannula (10)
• 05060696460064: Crawford 17 ga x 6” cannula (x10)