Knit-Pak

GUDID 00348783001914

Knit-Pak™ Knitted Retraction Size 3

PREMIER DENTAL PRODUCTS COMPANY

Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated Gingival retraction cord, non-medicated

• Primary Device ID: 00348783001914
• NIH Device Record Key: 67bf66e4-d70a-4635-80cc-5494856a3db6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Knit-Pak
• Version Model Number: 9007556
• Company DUNS: 014789663
• Company Name: PREMIER DENTAL PRODUCTS COMPANY
• 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: false
• Expiration Date: false
• 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	00348783001914 [Primary]

FDA Product Code

• NYF: Gingival Retraction Kit

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-01-10
• Device Publish Date: 2022-06-29

On-Brand Devices [Knit-Pak]

• D6919007559: SAMPLE – Knit-Pak™ Knitted Retraction Size 00 (19.7”)
• D6919007556: Knit-Pak™ Knitted Retraction Size 3
• D6919007555: Knit-Pak™ Knitted Retraction Size 2
• D6919007554: Knit-Pak™ Knitted Retraction Size 1
• D6919007553: Knit-Pak™ Knitted Retraction Size 0
• D6919007552: Knit-Pak™ Knitted Retraction Size 00
• D6919007551: Knit-Pak™ Knitted Retraction Size 000
• 00348783001921: SAMPLE – Knit-Pak™ Knitted Retraction Size 00 (19.7”)
• 00348783001914: Knit-Pak™ Knitted Retraction Size 3
• 00348783001907: Knit-Pak™ Knitted Retraction Size 2
• 00348783001891: Knit-Pak™ Knitted Retraction Size 1
• 00348783001884: Knit-Pak™ Knitted Retraction Size 0
• 00348783001877: Knit-Pak™ Knitted Retraction Size 00
• 00348783001860: Knit-Pak™ Knitted Retraction Size 000