Susol® Curette Double Ended 17cm

GUDID 05060418838683

BAILEY INSTRUMENTS LTD

General-purpose curette

• Primary Device ID: 05060418838683
• NIH Device Record Key: 4dd7a989-83a3-4d5a-bded-31eabfc4fbad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Susol® Curette Double Ended 17cm
• Version Model Number: SS62-4349
• Company DUNS: 769260357
• Company Name: BAILEY INSTRUMENTS LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060418838683 [Package]; Contains: 05060418838690; Package: Pack [10 Units]; In Commercial Distribution
GS1	05060418838690 [Primary]

FDA Product Code

• FZS: Curette, Surgical, General Use

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-31
• Device Publish Date: 2024-01-23

On-Brand Devices [Susol® Curette Double Ended 17cm]

• 05060418838683: SS62-4349
• 05060418836580: SS62-4349-F