Disposable Prep Razors

GUDID 00810180844901

Disposable Prep Razors

Dynarex Corporation

Safety razor, single-use

• Primary Device ID: 00810180844901
• NIH Device Record Key: 85151a3f-35a5-4621-9926-4155bde20547
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disposable Prep Razors
• Version Model Number: 4251
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 50
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616784425122 [Primary]
GS1	00616784425139 [Package]; Contains: 00616784425122; Package: [5 Units]; In Commercial Distribution
GS1	00810180844901 [Unit of Use]

FDA Product Code

• LWK: Razor, Surgical

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: 2026-03-25
• Device Publish Date: 2020-11-02

On-Brand Devices [Disposable Prep Razors]

• 00616784425115: Disposable Prep Razors
• 00810180844901: Disposable Prep Razors