Medical Action Industries Inc

GUDID 20809160270902

MEDICAL ACTION INDUSTRIES INC.

Surgical preparation kit

• Primary Device ID: 20809160270902
• NIH Device Record Key: 3673ba81-0adb-4c5a-9adf-c3b3e2ad3d7d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medical Action Industries Inc
• Version Model Number: 81048
• Company DUNS: 092364462
• Company Name: MEDICAL ACTION INDUSTRIES INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: true
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE

Device Identifiers

Device Issuing Agency	Device ID
GS1	10809160270905 [Primary]
GS1	20809160270902 [Package]; Contains: 10809160270905; Package: [20 Units]; In Commercial Distribution

FDA Product Code

• OJU: Skin prep tray

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-20
• Device Publish Date: 2019-11-12

On-Brand Devices [Medical Action Industries Inc]

• 20809160269845: 79916
• 20809160270360: 79817
• 20809160270919: LH_81045
• 20809160270902: 81048
• 20809160270896: 78318
• 20809160270889: 68549C
• 20809160270872: LH_79893B
• 20809160271510: 79612
• 20809160271756: 79299B
• 20809160271763: 79950