25169798

GUDID B34025169798

Pad Maxi ultra thin No. 4

IMPACT PRODUCTS, LLC

Menstrual pad, unscented

• Primary Device ID: B34025169798
• NIH Device Record Key: ca548cc1-214a-4c0f-84a1-a55d39ef85fb
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 25169798
• Catalog Number: 25169798
• Company DUNS: 005052360
• Company Name: IMPACT PRODUCTS, LLC
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B34025169798 [Primary]

FDA Product Code

• HHD: Pad, Menstrual, Unscented

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: 2020-06-12
• Device Publish Date: 2020-06-04

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