Denar Bite Wax

GUDID D040200000401

Wax, Dental, Intraoral

WHIP-MIX CORPORATION

Orthodontic appliance relief material

• Primary Device ID: D040200000401
• NIH Device Record Key: 9d0eaea2-4736-4a8e-9404-599323f041ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Denar Bite Wax
• Version Model Number: 20000040
• Company DUNS: 006385173
• Company Name: WHIP-MIX CORPORATION
• 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: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D040200000401 [Primary]

FDA Product Code

• EGD: Wax, Dental, Intraoral

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: 2023-08-28
• Device Publish Date: 2023-08-18

On-Brand Devices [Denar Bite Wax]

• DO40200000501: Wax, Dental, Intraoral
• D040200000401: Wax, Dental, Intraoral