Moretz

GUDID 00681490024778

PROSTHESIS 0563 MORETZ MALL TOTAL RIGHT

MEDTRONIC XOMED, INC.

Ossicular prosthesis, total

• Primary Device ID: 00681490024778
• NIH Device Record Key: b4e6d9e9-ccd9-441d-ad03-4d98852d2b4a
• Commercial Distribution Discontinuation: 2018-06-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Moretz
• Version Model Number: 0563
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00681490024778 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K885201

FDA Product Code

• ETA: REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-06-25

On-Brand Devices [Moretz]

• 00681490035460: PROSTHESIS 1156304 MORETZ PEG-TOP TOTAL
• 00681490024846: PROSTHESIS 0575 MORETZ CAM HD TOTAL
• 00681490024778: PROSTHESIS 0563 MORETZ MALL TOTAL RIGHT
• 00681490024754: PROSTHESIS 0562 MORETZ MALL TOTAL LEFT
• 20763000039763: VENT TUBE 1066177 10PK MORETZ TAB PAIR