Trophy Skin

GUDID 00851561006037

RejuvadermMD Microdemabrasion Device

TROPHY SKIN, INC

Dermabrasion brush, rotary

• Primary Device ID: 00851561006037
• NIH Device Record Key: 1fa782bd-fa6f-4d9b-9f92-8e525189d59f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trophy Skin
• Version Model Number: RejuvadermMD
• Company DUNS: 014294023
• Company Name: TROPHY SKIN, INC
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 866-546-4664
• Email: sales@trophyskin.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851561006037 [Primary]

FDA Product Code

• GFD: Dermatome

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-28
• Device Publish Date: 2016-09-06

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• 00851561006037: RejuvadermMD Microdemabrasion Device
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• 00851561006006: Microderm MD Home Microdermabrasion Machine
• 00851561006105: RejuvatoneMD Facial Toning Device