Medicine Cups 1oz

GUDID 00840117341210

Dynarex Corporation

Medicine cup, single-use

• Primary Device ID: 00840117341210
• NIH Device Record Key: 33e19911-9b5d-47bc-8a88-cf3d138e61e3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medicine Cups 1oz
• Version Model Number: 4252
• 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	00616784425238 [Primary]
GS1	00840117341210 [Unit of Use]

FDA Product Code

• KYW: Container, Liquid Medication, Graduated

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: 2024-11-05
• Device Publish Date: 2024-10-28

Devices Manufactured by Dynarex Corporation

• 00840117341210 - Medicine Cups 1oz: 2024-11-05
• 00840117341210 - Medicine Cups 1oz: 2024-11-05
• 00840117312906 - Resp-O2 Endotracheal Tube Cuffed, 4.0 mm: 2024-11-01 Sterile-EO
• 00840117312920 - Resp-O2 Endotracheal Tube Cuffed, 4.5 mm: 2024-11-01 Sterile-EO
• 00840117317475 - Resp-O2 Endotracheal Tube Cuffed, 5.0 mm: 2024-11-01 Sterile-EO
• 00840117312968 - Resp-O2 Endotracheal Tube Cuffed, 5.5 mm: 2024-11-01 Sterile-Eo
• 00840117312982 - Resp-O2 Endotracheal Tube Cuffed, 6.0 mm: 2024-11-01 Sterile-Eo
• 00840117313002 - Resp-O2 Endotracheal Tube Cuffed, 6.5 mm: 2024-11-01 Sterile-Eo
• 00840117313026 - Resp-O2 Endotracheal Tube Cuffed, 7.0 mm: 2024-11-01 Sterile-Eo