Elektra 582886

GUDID D7075828860

Elektra 25 g

IVOCLAR VIVADENT, INC.

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• Primary Device ID: D7075828860
• NIH Device Record Key: e872fe72-ed3b-47b3-aa19-e625df97aa5b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Elektra
• Version Model Number: 582886
• Catalog Number: 582886
• Company DUNS: 176935203
• Company Name: IVOCLAR VIVADENT, INC.
• 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: 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
HIBCC	D7075828860 [Primary]

FDA Product Code

• EJS: ALLOY, OTHER NOBLE METAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-04-27
• Device Publish Date: 2018-10-29

On-Brand Devices [Elektra]

• D7075828880: Elektra 100 g
• D7075828870: Elektra 1oz/31 g
• D7075828860: Elektra 25 g
• D7075828840: Elektra 5 g