HYBRIBOARD

GUDID 08057592700070

The sides of the Hybriboard do not expose the patient to the risk of secondary damage caused, as is the case with basket stretchers, by the vertical walls of the stretcher being 20-25cm high.

FLAMOR SRL

Portable stretcher

• Primary Device ID: 08057592700070
• NIH Device Record Key: 4beb20e6-2753-47fd-bda1-97dabf42be2c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HYBRIBOARD
• Version Model Number: EMS
• Company DUNS: 629852208
• Company Name: FLAMOR SRL
• 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: 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	08057592700070 [Primary]

FDA Product Code

• FPP: Stretcher, Hand-Carried

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: 2025-06-02
• Device Publish Date: 2025-05-23

On-Brand Devices [HYBRIBOARD]

• 08057592700087: The sides of the Hybriboard do not expose the patient to the risk of secondary damage caused, as
• 08057592700070: The sides of the Hybriboard do not expose the patient to the risk of secondary damage caused, as