GUDID ENTTR8101

Ti - Base Abutment

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

• Primary Device ID: ENTTR8101
• NIH Device Record Key: e4918ffb-676c-452a-8e1a-f45cab680cf3
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: R 810
• Company DUNS: 312800478
• Company Name: NT-Trading GmbH & Co. KG
• 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	ENTTR8101 [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

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

[ENTTR8101]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-08
• Device Publish Date: 2016-10-20

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