mateside

GUDID 06975960554020

Zhejiang Mateside Medical Devices Technology Co., Ltd

Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress

• Primary Device ID: 06975960554020
• NIH Device Record Key: b548dd04-d22b-4950-b287-403bc4b20d22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: mateside
• Version Model Number: S12A
• Company DUNS: 699411523
• Company Name: Zhejiang Mateside Medical Devices Technology Co., Ltd
• 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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	06975960554020 [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: 2023-03-13
• Device Publish Date: 2023-03-03

On-Brand Devices [mateside]

• 06975960551012: 901-HD
• 06975960551029: 901-LD
• 06975960551005: 901-BD
• 06975960554020: S12A
• 06975960554013: S11A