Temporary Abutment BH-SAT1

GUDID 07290109741772

Temporary Abutment - Hex

BHI IMPLANTS LTD

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07290109741772
• NIH Device Record Key: 0c2518e2-539b-4ad7-ab7f-bb373e7f05b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Temporary Abutment
• Version Model Number: 1
• Catalog Number: BH-SAT1
• Company DUNS: 600330916
• Company Name: BHI IMPLANTS LTD
• 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: false
• 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

Customer Support Contacts

• Phone: +972046094458
• Email: info@bh-implants.com

Device Dimensions

• Length: 12 Millimeter

Operating and Storage Conditions

• Handling Environment Temperature: Between 5 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109741772 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103280

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[07290109741772]

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: 2016-09-11

On-Brand Devices [Temporary Abutment ]

• 07290109741789: Temporary Abutment - NO Hex
• 07290109741772: Temporary Abutment - Hex