Susol® Partial Nail Avulsion Procedure Pack

GUDID 05060418834890

BAILEY INSTRUMENTS LTD

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• Primary Device ID: 05060418834890
• NIH Device Record Key: 1dbe0bc5-b3fa-46b0-98ea-ed516c54f314
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Susol® Partial Nail Avulsion Procedure Pack
• Version Model Number: BSDP-03
• 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	05060418833619 [Package]; Package: Pack [10 Units]; In Commercial Distribution
GS1	05060418834890 [Primary]

FDA Product Code

• KDD: Kit, Surgical Instrument, Disposable

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® Partial Nail Avulsion Procedure Pack]

• 05060418838409: BSDP-03-02-F
• 05060418836429: BSDP-03-F
• 05060418834890: BSDP-03