FEATHERVAC REUSABLE SUCTION

GUDID 00844505007115

FEATHERVAC REUSABLE SUCTION

Grace Medical, Inc.

Ossicular prosthesis introducer handpiece

• Primary Device ID: 00844505007115
• NIH Device Record Key: 477cd16b-f91c-4056-95e2-b20996cde891
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FEATHERVAC REUSABLE SUCTION
• Version Model Number: 906-001
• Company DUNS: 030849173
• Company Name: Grace Medical, Inc.
• Device Count: 1
• DM Exempt: true
• 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: false
• 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(866)472-2363
• Email: info@gracemedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00844505007115 [Primary]

FDA Product Code

• JZF: Tube, Ear Suction

Sterilization

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

[00844505007115]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-22
• Device Publish Date: 2018-09-21

On-Brand Devices [FEATHERVAC REUSABLE SUCTION]

• 00844505007115: FEATHERVAC REUSABLE SUCTION
• 00844505013918: FEATHERVAC REUSABLE SUCTION