Hemodent

GUDID 00348783001082

Hemodent® liquid 20cc, Pack of 10

PREMIER DENTAL PRODUCTS COMPANY

Gingival retraction solution

• Primary Device ID: 00348783001082
• NIH Device Record Key: 554fc5b2-4e90-4870-96ea-7babcb6a7fd1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hemodent
• Version Model Number: 9007072
• Company DUNS: 014789663
• Company Name: PREMIER DENTAL PRODUCTS COMPANY
• Device Count: 10
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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	00348783001082 [Unit of Use]
GS1	00348783001099 [Primary]

FDA Product Code

• MVL: Cord, Retraction
• NYF: Gingival Retraction Kit

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-21
• Device Publish Date: 2023-06-13

On-Brand Devices [Hemodent]

• 00348783001105: Hemodent® liquid 40cc, Pack of 10
• 00348783001082: Hemodent® liquid 20cc, Pack of 10
• 00348783001068: Hemodent® liquid 10cc, Pack of 10