Protection Products Inc.

GUDID 20809160242688

MEDICAL ACTION INDUSTRIES INC.

Infectious waste spill kit

• Primary Device ID: 20809160242688
• NIH Device Record Key: 3f18c441-720a-4e23-9736-f92e98eb38c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Protection Products Inc.
• Version Model Number: ERT0005B
• 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10809160242681 [Primary]
GS1	20809160242688 [Package]; Contains: 10809160242681; Package: [16 Units]; In Commercial Distribution

FDA Product Code

• MAC: Decontamination kit

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: 2019-06-19
• Device Publish Date: 2019-06-11

On-Brand Devices [Protection Products Inc.]

• 20809160242688: ERT0005B
• 20809160219000: ERT0005