mateside

GUDID 06976062570048

Hangzhou Guoyuan Yanglao 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: 06976062570048
• NIH Device Record Key: 344d078e-592d-4d8f-8f42-3e2f7e53e295
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: mateside
• Version Model Number: S12A
• Company DUNS: 844934699
• Company Name: Hangzhou Guoyuan Yanglao 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: false
• 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	06976062570048 [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: 2023-03-29
• Device Publish Date: 2023-03-21

On-Brand Devices [mateside]

• 06976062570055: S01A
• 06976062570048: S12A
• 06976062570031: S11A