Urinal- Male

GUDID 00810180844864

Urinal- Male, 1000c/1qt. , Transparent with Graduated Markings

Dynarex Corporation

Hand-held urinal, single-use

• Primary Device ID: 00810180844864
• NIH Device Record Key: 09e781dc-3b93-4f4b-9b2a-80372431d5b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Urinal- Male
• Version Model Number: 4229
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616784422930 [Primary]
GS1	00810180844864 [Unit of Use]

FDA Product Code

• FNP: Urinal

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 [Urinal- Male]

• 00616784422923: Urinal- Male, 1000c/1qt. , Transparent with Graduated Markings
• 00810180844864: Urinal- Male, 1000c/1qt. , Transparent with Graduated Markings