CoForm 604035

GUDID 17310236040351

Directa AB

Dental mould

• Primary Device ID: 17310236040351
• NIH Device Record Key: aea78930-8e9e-4b87-8d85-795cfb8aa9dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CoForm
• Version Model Number: Assortment A
• Catalog Number: 604035
• Company DUNS: 353954381
• Company Name: Directa AB
• 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	17310236040351 [Primary]

FDA Product Code

• ELZ: Crown, Preformed

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: 2022-12-15
• Device Publish Date: 2022-12-07

On-Brand Devices [CoForm ]

• 17310236040511: 41-42 Distal
• 17310236040504: 41-42 Mesial
• 17310236040498: 31-32 Distal
• 17310236040481: 31-32 Mesial
• 17310236040474: 23 Distal
• 17310236040467: 23 Mesial
• 17310236040450: 13 Distal
• 17310236040443: 13 Mesial
• 17310236040436: 22 Distal
• 17310236040429: 22 Mesial
• 17310236040412: 12 Distal
• 17310236040405: 12 Mesial
• 17310236040399: 21 Distal
• 17310236040382: 21 Mesial
• 17310236040375: 11 Distal
• 17310236040368: 11 Mesial
• 17310236040351: Assortment A
• 17310236040344: Assortment B