OptiCare X

GUDID 08592654271759

active integrated anti-decubitus mattresses

L I N E T spol. s r.o.

Alternating-pressure bed mattress overlay system

• Primary Device ID: 08592654271759
• NIH Device Record Key: 1baa929a-a641-49c4-8cc3-57cc427e5307
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OptiCare X
• Version Model Number: 1VSK0B0001000
• Company DUNS: 644544504
• Company Name: L I N E T spol. s r.o.
• 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: true
• 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	08592654271759 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-09
• Device Publish Date: 2021-11-01

On-Brand Devices [OptiCare X]

• 08592654271759: active integrated anti-decubitus mattresses
• 08592654363188: active integrated anti-decubitus mattresses
• 08592654394229: active integrated anti-decubitus mattresses