RS-Standard Internal Hex Plastic Surgical Kit-Adv

GUDID 07290105156365

ADIN DENTAL IMPLANT SYSTEMS LTD

Dental implant/prosthesis surgical procedure kit

• Primary Device ID: 07290105156365
• NIH Device Record Key: 099a9523-50bd-47fa-bd18-9b803d710e9c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RS-Standard Internal Hex Plastic Surgical Kit-Adv
• Version Model Number: RS6322IN
• 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	07290105156365 [Primary]

FDA Product Code

• OFY: Dental Implant Surgical Tray

Sterilization

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

[07290105156365]

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-Adv]

• 07290105156365: RS6322IN
• 07290105156358: RS6322