CurPro Undercast Padding, 100% Polyester, 8" x 4 yd

GUDID 00810180842129

Dynarex Corporation

Non-adhesive device retention bandage

• Primary Device ID: 00810180842129
• NIH Device Record Key: 086ea08a-7239-4908-aa74-1f1388d1fcce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CurPro Undercast Padding, 100% Polyester, 8" x 4 yd
• Version Model Number: 3889
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 20
• 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	00810180842129 [Unit of Use]
GS1	00840117344426 [Primary]
GS1	00840117344433 [Package]; Contains: 00840117344426; Package: Case [4 Units]; In Commercial Distribution

FDA Product Code

• ITG: Bandage, Cast

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: 2025-06-13
• Device Publish Date: 2025-06-05

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• 00616784191119 - DynaFit Graduated Compression Anti-Embolism Stocking, Medium Knee: 2025-10-06
• 00616784191218 - DynaFit Graduated Compression Anti-Embolism Stocking, Large Knee: 2025-10-06
• 00616784191317 - DynaFit Graduated Compression Anti-Embolism Stocking, X-Large Knee: 2025-10-06