MyOstomy

GUDID 20860010399709

Ostomy Suction Device, 22.5mm

Myostomy Distribution LLC

Cupping therapy device

• Primary Device ID: 20860010399709
• NIH Device Record Key: 2abff701-ca90-4617-a51e-b09506285f62
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MyOstomy
• Version Model Number: G4772250
• Company DUNS: 120805657
• Company Name: Myostomy Distribution 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860010399705 [Primary]
GS1	20860010399709 [Package]; Contains: 00860010399705; Package: [1 Units]; In Commercial Distribution

FDA Product Code

• GCY: Apparatus, Suction, Single Patient Use, Portable, Nonpowered

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: 2023-09-22
• Device Publish Date: 2023-09-14

On-Brand Devices [MyOstomy]

• 20860010399716: Ostomy Suction Device, 25mm
• 20860010399709: Ostomy Suction Device, 22.5mm