Mark II Plus Articulator 110500-3

GUDID D04011050031

A dental articulator is a device designed to simulate all or part of the mandibular movements and used for examination, diagnosis, or to construct dental appliances. This is a reusable device.

WHIP-MIX CORPORATION

Dental articulator

• Primary Device ID: D04011050031
• NIH Device Record Key: b5817147-47e0-46b8-a67f-1257bc2975ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mark II Plus Articulator
• Version Model Number: 110500-3
• Catalog Number: 110500-3
• 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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
HIBCC	D04011050031 [Primary]

FDA Product Code

• EJP: Articulators

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: 2020-09-30
• Device Publish Date: 2020-09-22

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