GUDID 00673978230467

CATHETER 81192 ALGOLINE W CLOSED TIP

MEDTRONIC PS MEDICAL, INC.

Spinal infusion/drainage catheter

• Primary Device ID: 00673978230467
• NIH Device Record Key: 0e87baf2-d398-45bc-b6a3-7e18d448caaa
• Commercial Distribution Discontinuation: 2017-03-06
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 81192
• Company DUNS: 089055867
• Company Name: MEDTRONIC PS MEDICAL, INC.
• 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: false
• 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(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Length: 80 Centimeter
• Length: 80 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00673978230467 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K911382

FDA Product Code

• MAJ: CATHETER, PERCUTANEOUS, INTRASPINAL, SHORT TERM

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: 2018-07-06
• Device Publish Date: 2015-12-03

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