UF(II) Eco Bite Impression Coping

GUDID 08800049432358

DIO Corporation

Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 08800049432358
• NIH Device Record Key: 0d61de28-ded2-4a19-9d40-f83e88d49d2f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UF(II) Eco Bite Impression Coping
• Version Model Number: USBI 4804H
• Company DUNS: 631085206
• Company Name: DIO Corporation
• Device Count: 1
• DM Exempt: true
• 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: true
• 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
GS1	08800049432358 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

[08800049432358]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-11
• Device Publish Date: 2023-09-01

On-Brand Devices [UF(II) Eco Bite Impression Coping]

• 08800049442845: USBI 4504H
• 08800049436325: USNBI 4204H
• 08800049432372: USBI 6504H
• 08800049432365: USBI 5504H
• 08800049432358: USBI 4804H
• 08800049431771: USNBI 4004H