CENTERED ALTO PARTIAL 10MM L

GUDID 00844505011563

CENTERED ALTO PARTIAL 10MM LENGTH TITANIUM/SILICONE

Grace Medical, Inc.

Ossicular prosthesis, partial

• Primary Device ID: 00844505011563
• NIH Device Record Key: 966e07ae-e08e-4fa9-944c-6caff195db88
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CENTERED ALTO PARTIAL 10MM L
• Version Model Number: 655-M2
• Company DUNS: 030849173
• Company Name: Grace Medical, Inc.
• Device Count: 1
• DM Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)472-2363
• Email: info@gracemedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00844505011563 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061853

FDA Product Code

• ETB: Prosthesis, Partial Ossicular Replacement

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: 2017-10-16

On-Brand Devices [CENTERED ALTO PARTIAL 10MM L]

• 00844505011563: CENTERED ALTO PARTIAL 10MM LENGTH TITANIUM/SILICONE
• 00844505013215: CENTERED ALTO PARTIAL 10MM SIZERS INCLUDED LENGTH TITANIUM/SILICONE