luxaprint 3D shell UV beige 1000 g

GUDID EDET035131

DETAX GmbH & Co. KG

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• Primary Device ID: EDET035131
• NIH Device Record Key: a3dc8e90-cf62-450c-97ea-a520c1c7513f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: luxaprint 3D shell UV beige 1000 g
• Version Model Number: 03513
• Company DUNS: 317099257
• Company Name: DETAX GmbH & Co. KG
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EDET035131 [Primary]

FDA Product Code

• ESD: Hearing Aid, Air-Conduction, Prescription

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: 2022-11-02
• Device Publish Date: 2022-10-25

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