GUDID EGEB211081

TRIBOS 501 Kunststoffzaehne SM-UK-B3

Gebdi Dental-Products GmbH

Partial denture

• Primary Device ID: EGEB211081
• NIH Device Record Key: a0aa8978-ee4c-4492-b621-20ca51556ec7
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 21108
• Company DUNS: 342656675
• Company Name: Gebdi Dental-Products GmbH
• Device Count: 1
• DM Exempt: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +497733941016
• Email: info@gebdi-dental.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EGEB211081 [Primary]

FDA Product Code

• ELM: Denture, plastic, teeth

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: 2018-03-29
• Device Publish Date: 2016-10-25

Devices Manufactured by Gebdi Dental-Products GmbH

• EGEB200011 - NA: 2018-03-29 TRIBOS 501 Kunststoffzaehne PM-OK-A1
• EGEB200021 - NA: 2018-03-29 TRIBOS 501 Kunststoffzaehne PM-OK-A2
• EGEB200031 - NA: 2018-03-29 TRIBOS 501 Kunststoffzaehne PM-OK-A3
• EGEB200041 - NA: 2018-03-29 TRIBOS 501 Kunststoffzaehne PM-OK-A3,5
• EGEB200051 - NA: 2018-03-29 TRIBOS 501 Kunststoffzaehne PM-OK-A4
• EGEB200061 - NA: 2018-03-29 TRIBOS 501 Kunststoffzaehne PM-OK-B1
• EGEB200071 - NA: 2018-03-29 TRIBOS 501 Kunststoffzaehne PM-OK-B2
• EGEB200081 - NA: 2018-03-29 TRIBOS 501 Kunststoffzaehne PM-OK-B3