SOLEIL

GUDID 00366975010810

SOLEIL SUPREME LED SLEEVE 250

BENCO DENTAL SUPPLY CO.

Cable/lead/sensor/probe cover, non-sterile

• Primary Device ID: 00366975010810
• NIH Device Record Key: c01c8d14-8117-4a3e-8d1c-5ad4c426617b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SOLEIL
• Version Model Number: 4950-145
• Company DUNS: 015108087
• Company Name: BENCO DENTAL SUPPLY CO.
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Dimensions

• Length: 10.39 Inch
• Length: 10.39 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00366975010810 [Primary]

FDA Product Code

• PEM: Dental Barriers And Sleeves

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-11-13

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