Pill Crusher Pouch

GUDID 00840117350045

Pill Crusher Pouch

Dynarex Corporation

Pill crusher/splitter

• Primary Device ID: 00840117350045
• NIH Device Record Key: 7edb8187-f38b-4ead-94b4-28667d597123
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pill Crusher Pouch
• Version Model Number: 4210
• 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: false
• 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	00810180844833 [Unit of Use]
GS1	00840117350045 [Primary]
GS1	00840117350052 [Package]; Package: Case [20 Units]; In Commercial Distribution

FDA Product Code

• OHY: Pill Crusher/Cutter

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: 2026-03-24
• Device Publish Date: 2021-09-01

On-Brand Devices [Pill Crusher Pouch]

• 00616784421025: Pill Crusher Pouch
• 00840117350045: Pill Crusher Pouch