Alternating Pressure Mattress

GUDID 00851675007180

Alternating Pressure Mattress (2 bladder)

CORK MEDICAL, LLC

Alternating-pressure bed mattress overlay system

• Primary Device ID: 00851675007180
• NIH Device Record Key: 3e17fe12-f2e1-43f6-b506-5b5bc828a38d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alternating Pressure Mattress
• Version Model Number: CMP-6000
• Company DUNS: 015964214
• Company Name: CORK MEDICAL, 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: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851675007180 [Primary]

FDA Product Code

• FNM: Mattress, Air Flotation, Alternating Pressure

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: 2018-03-29
• Device Publish Date: 2016-09-02

On-Brand Devices [Alternating Pressure Mattress]

• 00851675007197: Alternating Pressure Mattress (3 bladder)
• 00851675007180: Alternating Pressure Mattress (2 bladder)