L-560B

GUDID 10841336100494

SALVIN 3-0 CHROMIC GUT C6(FS-2) NEEDLE 27" (68CM)

Salvin Dental Specialties, Inc.

Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic Catgut suture, chromic

• Primary Device ID: 10841336100494
• NIH Device Record Key: 5aa3e0cf-66c3-4461-96d0-e7956c7eea22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: L-560B
• Version Model Number: L-560B
• Company DUNS: 113344790
• Company Name: Salvin Dental Specialties, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Expiration Date: true
• 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	00841336100497 [Primary]
GS1	10841336100494 [Package]; Contains: 00841336100497; Package: [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K896554

FDA Product Code

• GAL: Suture, Absorbable, Natural

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-10-30

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