RAYDENT SG

GUDID 08800003006151

Ray Co., Ltd

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• Primary Device ID: 08800003006151
• NIH Device Record Key: 0cc3f858-ffcc-4f66-a06e-27f230d0aa2d
• Commercial Distribution Discontinuation: 2022-11-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: RAYDENT SG
• Version Model Number: RSG0QB
• Company DUNS: 690324087
• Company Name: Ray Co., 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800003006151 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-11
• Device Publish Date: 2022-11-03

On-Brand Devices [RAYDENT SG]

• 18800003006134: RSG05P
• 18800003006127: RSG04P
• 18800003006110: RSG03P
• 18800003006103: RSG02P
• 18800003006097: RSG01P
• 08800003006175: RSG10B
• 08800003006168: RSG05B
• 08800003006151: RSG0QB
• 08800003006144: RSG02B