DMI 552-1982-0000

GUDID 10041298019821

PRESSURE PAD ALTERNATING ONLY 32 X 72 IN INFLATED

D-M-S HOLDINGS, INC.

Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use Alternating-pressure chair cushion, single-use

• Primary Device ID: 10041298019821
• NIH Device Record Key: 61293738-aa6a-4af2-ba25-c3b7988f6c25
• Commercial Distribution Discontinuation: 2023-05-17
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: DMI
• Version Model Number: 552-1982-0000
• Catalog Number: 552-1982-0000
• Company DUNS: 062028220
• Company Name: D-M-S HOLDINGS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00041298019824 [Primary]
GS1	10041298019821 [Package]; Contains: 00041298019824; Package: Master Carton [10 Units]; Discontinued: 2023-05-17; Not in Commercial Distribution

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: 3
• Public Version Date: 2023-05-18
• Device Publish Date: 2016-09-23

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