BegoPal+ 61550

GUDID EBGO615501

BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG

Dental casting non-noble alloy

• Primary Device ID: EBGO615501
• NIH Device Record Key: 3a0b279d-8e07-45e9-b262-d19872a5a80c
• Commercial Distribution Discontinuation: 2017-05-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: BegoPal+
• Version Model Number: 61550
• Catalog Number: 61550
• 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

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EBGO615501 [Primary]

FDA Product Code

• EJH: Alloy, Metal, Base

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-04-26
• Device Publish Date: 2016-11-15

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