RS-Standard Internal Hex Plastic Surgical Kit-Prem

GUDID 07290105156310

ADIN DENTAL IMPLANT SYSTEMS LTD

Dental implant/prosthesis surgical procedure kit

• Primary Device ID: 07290105156310
• NIH Device Record Key: 2447f429-135d-4df3-9021-a40e9d3a4fda
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RS-Standard Internal Hex Plastic Surgical Kit-Prem
• Version Model Number: RS6301
• Company DUNS: 533289435
• Company Name: ADIN DENTAL IMPLANT SYSTEMS LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• 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	07290105156310 [Primary]

FDA Product Code

• OFY: Dental Implant Surgical Tray

Sterilization

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

[07290105156310]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-04-23

On-Brand Devices [RS-Standard Internal Hex Plastic Surgical Kit-Prem]

• 07290105156327: RS6301IN
• 07290105156310: RS6301