Hydrodebrider®

GUDID 00643169376106

HYDRODEBRIDER 1914001 STD HANDPIECE ROHS

MEDTRONIC XOMED, INC.

Nasal lavage system

• Primary Device ID: 00643169376106
• NIH Device Record Key: f6753cf3-fd48-4fa8-b8d3-03a9cf6b68b9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hydrodebrider®
• Version Model Number: 1914001
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00643169376106 [Primary]

FDA Product Code

• KMA: IRRIGATOR, POWERED NASAL

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: 2018-03-29
• Device Publish Date: 2017-10-13

On-Brand Devices [Hydrodebrider®]

• 00613994712608: HANDPIECE 1921002 HYDRODEBRID FRNTL ROHS
• 00613994233332: HYDRODEBRIDER 1914001 STANDARD HANDPIECE
• 00613994233295: CONSOLE 1913001 HYDRODEBRIDER
• 00643169376106: HYDRODEBRIDER 1914001 STD HANDPIECE ROHS
• 00643169360877: CONSOLE 1913001 HYDRODEBRIDER ROHS
• 00763000089597: CONSOLE 1913001 HYDRODEBRIDER