K2 OPAQUER powder, O-A2, 50g

GUDID EYET3205002

Yeti Dentalprodukte GmbH

Dental appliance fabrication material, ceramic

• Primary Device ID: EYET3205002
• NIH Device Record Key: 4300dd58-dff9-4c55-9e7e-16dca3f61d17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K2 OPAQUER powder, O-A2, 50g
• Version Model Number: 320-5002
• Company DUNS: 324001916
• Company Name: Yeti Dentalprodukte GmbH
• 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: true
• 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	EYET3205002 [Primary]

FDA Product Code

• EIH: Powder, Porcelain

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: 2025-05-01
• Device Publish Date: 2025-04-23

Devices Manufactured by Yeti Dentalprodukte GmbH

• EYET3201501 - K2 OPAQUER powder, O-A1, 15g.: 2025-05-01
• EYET3201502 - K2 OPAQUER powder, O-A2, 15g.: 2025-05-01
• EYET3201503 - K2 OPAQUER powder, O-A3, 15g.: 2025-05-01
• EYET3201504 - K2 OPAQUER powder, O-A3,5, 15g: 2025-05-01
• EYET3201505 - K2 OPAQUER powder, O-A4, 15g.: 2025-05-01
• EYET3201506 - K2 OPAQUER powder, O-B1, 15g: 2025-05-01
• EYET3201507 - K2 OPAQUER powder, O-B2, 15g: 2025-05-01
• EYET3201508 - K2 OPAQUER powder, O-B3, 15g.: 2025-05-01