Protection Products Inc.

GUDID 20809160219000

MEDICAL ACTION INDUSTRIES INC.

Infectious waste spill kit

• Primary Device ID: 20809160219000
• NIH Device Record Key: f088a880-b5dd-4f01-9f14-e7b766884952
• Commercial Distribution Discontinuation: 2019-07-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Protection Products Inc.
• Version Model Number: ERT0005
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10809160219003 [Primary]
GS1	20809160219000 [Package]; Contains: 10809160219003; Package: [16 Units]; Discontinued: 2019-07-10; Not 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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-07-11
• Device Publish Date: 2018-11-19

On-Brand Devices [Protection Products Inc.]

• 20809160242688: ERT0005B
• 20809160219000: ERT0005