Ellis Instruments, Inc.

GUDID 00860007290664

Ellis Instruments Inc

Surgical implant handling forceps

• Primary Device ID: 00860007290664
• NIH Device Record Key: 6bf985c0-baa1-4705-abbb-8ebca7f835de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ellis Instruments, Inc.
• Version Model Number: #125-815
• Company DUNS: 926867201
• Company Name: Ellis Instruments 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860007290664 [Primary]

FDA Product Code

• GEN: Forceps, General & Plastic Surgery

Sterilization

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

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

[00860007290664]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-15
• Device Publish Date: 2021-11-05

On-Brand Devices [Ellis Instruments, Inc. ]

• 00860007290664: #125-815
• 00860007290640: #125-080
• 00860007290626: #125-025
• 00860007290602: #125-024