Permanent Crown A2

GUDID EBGOFLPCA201

BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG

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• Primary Device ID: EBGOFLPCA201
• NIH Device Record Key: 3cd03ca5-8f42-4e52-8fb5-0ed1bd6b6a3e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Permanent Crown A2
• Version Model Number: FLPCA201US
• Company DUNS: 316483072
• Company Name: BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• 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

Customer Support Contacts

• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com
• Phone: +4942120280
• Email: info@bego.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry
• Special Storage Condition, Specify: Between 0 and 0 *Dry

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EBGOFLPCA201 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201668

FDA Product Code

• EBF: Material, Tooth Shade, Resin

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: 2020-10-27
• Device Publish Date: 2020-10-19

On-Brand Devices [Permanent Crown A2]

• EBGOFLPCA201: FLPCA201US
• EBGOFLPCA201US1: FLPCA201US