Emesis Basin

GUDID 00616784422428

Emesis Basin, 9", Graduated in 100cc, Mauve

DYNAREX CORPORATION

Emesis bowl, reusable

• Primary Device ID: 00616784422428
• NIH Device Record Key: 61ef1a91-5566-46d5-93ee-73f6aa5e0e33
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Emesis Basin
• Version Model Number: 4224
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 250
• 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: false
• Lot Batch: false
• 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	00616784422428 [Unit of Use]
GS1	00616784422435 [Primary]

FDA Product Code

• FNY: Basin, Emesis

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: 2022-05-10
• Device Publish Date: 2022-05-02

On-Brand Devices [Emesis Basin]

• 00616784422428: Emesis Basin, 9", Graduated in 100cc, Mauve
• 00810180844840: Emesis Basin, 9", Graduated in 100cc, Mauve