Screw for Multi Unit HEX Implant BH-MUIS

GUDID 07290109742106

Screw for Multi Unit HEX Implant

BHI IMPLANTS LTD

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07290109742106
• NIH Device Record Key: 0ee8e96c-ae88-4875-b826-842ea0fb4191
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Screw for Multi Unit HEX Implant
• Version Model Number: 1
• Catalog Number: BH-MUIS
• 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

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109742106 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103280

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

[07290109742106]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-12-24
• Device Publish Date: 2019-12-16

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• 07290109747637 - ROSEN SCREW: 2024-06-28 50 X Rosen Screw UNF 1.72 (T5)
• 07290109747644 - ROSEN SCREW: 2024-06-28 50 X Wave Rosen Screw UNF 1.72 (T5)