W.O.W.™

GUDID 00348783005813

WSL DIE MAKERS ARTICULATOR (BAG 50)

PREMIER DENTAL PRODUCTS COMPANY

Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator Dental articulator

• Primary Device ID: 00348783005813
• NIH Device Record Key: 29025c45-cd25-41fa-ada1-36f15d137698
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: W.O.W.™
• Version Model Number: 0020
• 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: 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
GS1	00348783005813 [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: 2024-06-14
• Device Publish Date: 2024-06-06

On-Brand Devices [W.O.W.™]

• 00348783005844: WOW ARTIC POSTERIOR ORIGINAL-50
• 00348783005837: WOW DOWEL PINS (BAG 300)
• 00348783005820: WOW ARTIC FULL ARCH ORIGINAL-50
• 00348783005813: WSL DIE MAKERS ARTICULATOR (BAG 50)