Susol® Micro Curette Double Ended with hole

GUDID 05060418836689

BAILEY INSTRUMENTS LTD

General-purpose curette

• Primary Device ID: 05060418836689
• NIH Device Record Key: 6bf8053a-ed0d-4e1c-b2ac-9b759d52b7f3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Susol® Micro Curette Double Ended with hole
• Version Model Number: SS62-4300-F
• 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	05060418836672 [Primary]
GS1	05060418836689 [Package]; Contains: 05060418836672; Package: Pack [10 Units]; In Commercial Distribution

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® Micro Curette Double Ended with hole]

• 05060418836689: SS62-4300-F
• 05060418836177: SS62-4300