ECLIPSE TITANIUM PISTON

GUDID 00844505006705

ECLIPSE TITANIUM PISTON 0.5MM DIA X 4.50MM L NITINOL/TITANIUM

Grace Medical, Inc.

Ossicular prosthesis, partial

• Primary Device ID: 00844505006705
• NIH Device Record Key: 21e7e784-13f4-4fbb-b624-0ce8fec1a4e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ECLIPSE TITANIUM PISTON
• Version Model Number: 470-450
• Company DUNS: 030849173
• Company Name: Grace Medical, Inc.
• Device Count: 1
• DM Exempt: true
• 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: 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

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 and 140 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00844505006705 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K063374

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: 4
• Public Version Date: 2020-05-04
• Device Publish Date: 2016-02-18

On-Brand Devices [ECLIPSE TITANIUM PISTON]

• 00844505006712: ECLIPSE TITANIUM PISTON 0.5MM DIA X 4.75MM L NITINOL/TITANIUM
• 00844505006705: ECLIPSE TITANIUM PISTON 0.5MM DIA X 4.50MM L NITINOL/TITANIUM
• 00844505006699: ECLIPSE TITANIUM PISTON 0.5MM DIA X 4.25MM L NITINOL/TITANIUM
• 00844505006682: ECLIPSE TITANIUM PISTON 0.5MM DIA X 4.00MM L NITINOL/TITANIUM