THO 80400000

GUDID ENTTTHO804000001

NT-Trading GmbH & Co. KG

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed

• Primary Device ID: ENTTTHO804000001
• NIH Device Record Key: 73b806da-23bd-4ae6-a442-160dc78212c6
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: THO 80400000
• Catalog Number: THO 80400000
• Company DUNS: 312800478
• Company Name: NT-Trading GmbH & Co. KG
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
HIBCC	ENTTTHO804000001 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111935

FDA Product Code

• NHA: ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

[ENTTTHO804000001]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-08
• Device Publish Date: 2019-08-23

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• ENTTBEG9S3D32371 - -: 2023-07-31 Scanbody 3D-Guide®
• ENTTBEG9S3D41001 - -: 2023-07-31 Scanbody 3D-Guide®
• ENTTBEG9S3D45001 - -: 2023-07-31 Scanbody 3D-Guide®